Extracurricular laboratory: Synthetic route of 2-Methylpropane-1,2-diol

According to the analysis of related databases, 558-43-0, the application of this compound in the production field has become more and more popular.

Related Products of 558-43-0, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 558-43-0, name is 2-Methylpropane-1,2-diol. This compound has unique chemical properties. The synthetic route is as follows.

Example 1 (not in Accordance with the Present Invention) Synthesis of the 2-hydroxy-2-methylpropyl Acrylate Precursor Under inert gas, triethylamine (66.8 g, 91.5 mL, 0.66 mol, 1.2 eq.) and 2-methylpropane-1,2-diol (49.6 g, 0.55 mol, 1 eq.) are initially charged in 300 mL of dichloromethane and cooled to 0 C. with an ice bath. A solution of 200 mL of dichloromethane and acryloyl chloride (49.8 g, 44.5 mL, 0.55 mol, 1 eq.) is added dropwise at room temperature via a dropping funnel in the course of an hour. A colorless precipitate was gradually formed in the course of the dropwise addition. The reaction solution was warmed to room temperature overnight and then the resultant precipitate was filtered off. The reaction solution was washed twice with 100 mL of water each time and dried over MgSO4. Then, the solvent was removed in a rotary evaporator and the crude product was distilled in vacuo. Boiling point 43-44 C./7.7-8.4 10-1 mbar. This gave 50.7 g (71%) of the pure product as a colorless clear liquid, storage at 7 C., stabilized with 4-methoxyphenol. 1H NMR (CDCl3): delta=1.21 (s, 6H, CH3), 2.30 (br s, 1H, OH), 3.99 (s, 2H, CH2), 5.81 (dd, 3JH,H=10.5 Hz, 1.5 Hz, 1H) 6.12 (dd, 3JH,H=10.5 Hz, 1.7 Hz, 1H), 6.39 ppm (dd, 3JH,H=1.5 Hz, 17 Hz, 1H). 13C NMR (CDCl3): delta=26.05 (2C, CH3), 69.72 (1C, COH), 72.01 (1C, CH2), 127.99 (1C, HC?CH2), 131.19 (1C, HC?CH2), 166.08 ppm (1C, ROC?O).

According to the analysis of related databases, 558-43-0, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Wacker Chemie AG; FRITZ-LANGHALS, Elke; (7 pag.)US2018/201633; (2018); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Simple exploration of 2-Methylpropane-1,2-diol

The chemical industry reduces the impact on the environment during synthesis 558-43-0, I believe this compound will play a more active role in future production and life.

Application of 558-43-0, With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.558-43-0, name is 2-Methylpropane-1,2-diol, molecular formula is C4H10O2, molecular weight is 90.121, as common compound, the synthetic route is as follows.

General procedure: To a 50 mL flask, the coumarin (1 mmol), appropriate amount of NXS, the Lewisacid catalyst and 20 mL anhydrous solvent were added in. The mixture was heated toreflux with a condenser under the protection of a drying tube. The reaction progresswas monitored by TLC. When the reaction was completed, the mixture was cooled toroom temperature. The solvent was removed by vacuum rotary evaporation, and theresidue was dispensed in 25 mL 5% sodium hydrogen sulfite (NaHSO3) aqueoussolution and then extracted with 25 mL ethyl acetate (EtOAc) for three times. Theorganic layer was combined, washed with 10 mL water and dried over anhydroussodium sulphate (Na2SO4). After the solvent was removed, the crude product waspurified by silica gel (300-400 mesh) column chromatograph.

The chemical industry reduces the impact on the environment during synthesis 558-43-0, I believe this compound will play a more active role in future production and life.

Reference:
Article; Su, Jinling; Zhang, Yan; Chen, Mingren; Li, Weiming; Qin, Xuewei; Xie, Yanping; Qin, Lixiao; Huang, Shihua; Zhang, Min; Synlett; vol. 30; 5; (2019); p. 630 – 634;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Top Picks: new discover of C4H11NO

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 2854-16-2, in my other articles. Product Details of 2854-16-2.

Chemistry is an experimental science, Product Details of 2854-16-2, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 2854-16-2, Name is 1-Amino-2-methylpropan-2-ol, molecular formula is C4H11NO, belongs to alcohols-buliding-blocks compound. In a document, author is Chen, Qifeng.

Traditional wound dressings have some major deficiencies, including poor antibacterial ability, low exudate absorption rate and dry environment. These defects can be addressed by the prepared hydrogels in this study, which can provide a moist and cool environment for wound healing. Polyvinyl alcohol-chitosan/cerium (PVA-Cs/Ce) composite hydrogels are prepared by a freeze-thaw method and characterized by x-ray diffraction (XRD) and scanning electron microscopy (SEM). In addition, the effects of chitosan/cerium (Cs/Ce) complexes with different contents on properties, including mechanical properties, water vapor permeability, swelling ratio, and thermal stability are investigated. SEM images indicate that the composite hydrogels have a good three-dimensional pore structure. Compared with the pure PVA hydrogel, the composite hydrogels show better swelling properties and more suitable water vapor transmission rate (2504 g m(-2).day) by adding Cs/Ce complexes. And the elongation at break of the hydrogel with a ratio of 5:3 (PVA: Cs/Ce) is the highest value of 567%. In the bacteriostatic circle experiment, PVA-Cs/Ce composite hydrogels exhibit a pronounced inhibitory effect against two bacteria (Staphylococcus aureus and Escherichia coli). These results suggest that these composite hydrogels have great potential as wound dressings.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 2854-16-2, in my other articles. Product Details of 2854-16-2.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Simple exploration of 3-Aminopropan-1-ol

Application of 156-87-6, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 156-87-6 is helpful to your research.

Application of 156-87-6, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, 156-87-6, Name is 3-Aminopropan-1-ol, SMILES is OCCCN, belongs to alcohols-buliding-blocks compound. In a article, author is Abdelmigeed, Mai O., introduce new discover of the category.

A magnetized zeolitic imidazolate framework (ZIF-8) impregnated with sodium hydroxide catalyst has been synthesized and tested as a new catalyst for biodiesel production. The new catalyst was investigated for the ethanolysis of vegetable oil to produce biodiesel. The operating conditions of the biodiesel production were optimized using the 2n design method followed by a reduced number of experimental runs. A 70% conversion of oil in the ethanolysis reaction was achieved using the new catalyst. The optimized operating conditions were found to be alcohol to oil molar ratio of 21:1, catalyst loading of 1% wt., a reaction time of 90 min, and temperature of 75 degrees C. Ethanolysis reaction was found to obey the pseudosecond-order kinetic model. In addition, the Arrhenius pre-exponential constant and activation energy were calculated to be 1.12 x 10(10) L mol(-1).min(1) and 77.27 kJ/mol, respectively. The physical properties of the product biodiesel matched the American Society for Testing and Materials (ASTM) ranges. Additionally, the product biodiesel achieved a Cetane number of 75, which is 15% higher than the upper range of the ASTM. (C) 2020 Elsevier Ltd. All rights reserved.

Application of 156-87-6, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 156-87-6 is helpful to your research.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Extracurricular laboratory: Discover of 2516-33-8

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 2516-33-8, in my other articles. Name: Cyclopropylmethanol.

Chemistry is an experimental science, Name: Cyclopropylmethanol, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 2516-33-8, Name is Cyclopropylmethanol, molecular formula is C4H8O, belongs to alcohols-buliding-blocks compound. In a document, author is Roche, Ann.

Objective Older workers are increasingly prevalent in health and human services, including the alcohol and other drug (AOD) sector. Their turnover intentions have important implications for service system stability and retention. Methods Descriptive and regression analyses of survey data examined age-related differences (<50, >= 50 years old) in non-government workers’ demographic, health and professional profiles and predictors of turnover intention. Results Older workers (>= 50 years, n = 86) comprised one-third of this workforce. Compared to younger workers (n = 164), they experienced greater discrimination but higher work-life balance and work engagement. Turnover intention was predicted by job satisfaction, discrimination and work engagement. Conclusion Older workers’ well-being and workforce retention are essential for effective leadership, succession planning and service continuity. Their needs and retention motivations are identified. Age-specific support mechanisms, proactive retention and anti-discrimination strategies are identified priorities.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 2516-33-8, in my other articles. Name: Cyclopropylmethanol.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

New downstream synthetic route of 56-81-5

At the same time, in my other blogs, there are other synthetic methods of this type of compound,56-81-5, Propane-1,2,3-triol, and friends who are interested can also refer to it.

With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.56-81-5, name is Propane-1,2,3-triol, molecular formula is C3H8O3, molecular weight is 92.0938, as common compound, the synthetic route is as follows.Computed Properties of C3H8O3

Will be 920g of glycerin,990gParaformaldehyde and20 g of the supported solid super acid catalyst prepared in Example 2 was addedIn the reaction device, the reaction is heated to 80 C, and the water having a lower boiling point and the trioxane formed in the reaction process enters the fractionation device.According to the principle that the boiling point of paraformaldehyde is lower than water, the triacetal is fractionated back to the reaction unit through a fractionation device.The reaction was carried out as a raw material, and the reaction was completed for 5 hours to obtain glycerol formal, and the product was analyzed by HPLC-MS.At 96.3%, the ratio of the six-membered ring product to the product of the five-membered ring in the product was 70:25.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,56-81-5, Propane-1,2,3-triol, and friends who are interested can also refer to it.

Reference:
Patent; Zhejiang Haotang Industrial Co., Ltd.; Liu Demin; (5 pag.)CN109535122; (2019); A;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

28-Sep News The important role of 927-74-2

The synthetic route of 927-74-2 has been constantly updated, and we look forward to future research findings.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 927-74-2, name is 3-Butyn-1-ol, the common compound, a new synthetic route is introduced below. Quality Control of 3-Butyn-1-ol

Preparation 39 Methyl [4-(4-Hydroxybut-1-ynyl)phenyl]acetate To a stirred solution of the product of Preparation 38 (4.5 g, 16.3 mmol) in diethylamine (100 mL) was added but-3-yn-1-ol (1.9 mL, 32.6 mmol), Pd(PPh3)2Cl2 (500 mg, 1.63 mmol) and CuI (154 mg, 0.815 mmol) and resulting mixture was stirred for 17 h at room temperature. The solvent was then removed under reduced pressure and the residue was dissolved in diethyl ether (200 mL) and this solution was filtered to remove salts. The solvent was then removed under reduced pressure and the crude product was purified by silica gel chromatography (60% EtOAc/Hexane) to afford the title intermediate (3.03 g, 91% yield).

The synthetic route of 927-74-2 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Mammen, Mathai; Dunham, Sarah; US2005/113417; (2005); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

9/28 News Brief introduction of 534-03-2

According to the analysis of related databases, 534-03-2, the application of this compound in the production field has become more and more popular.

Electric Literature of 534-03-2, Adding some certain compound to certain chemical reactions, such as: 534-03-2, name is 2-Aminopropane-1,3-diol,molecular formula is C3H9NO2, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 534-03-2.

General procedure: A stirred solution of 2-amino-1,3-propanediol (serinol) 4 (1 eq) and triethylamine (TEA) inMeOH (10 mL) was cooled at -20 C (carbon dioxide snow) and added dropwise a solutionof the corresponding acyl chloride (1.1 eq) in THF (5 mL). The reaction mixture was allowed towarm to room temperature and stirred overnight. Then it was poured into brine and extractedwith dichloromethane (3 10 mL). The combined organic phases were washed with brine, driedover MgSO4 and concentrated under reduced pressure. The residue was purified by flash columnchromatography on silica gel using as eluent EtOAc/MeOH (20:1 to 7:1) to provide the correspondingN-acyl serinol derivatives. 4.1.4. N-octanoyl Serinol (5)According to the general procedure serinol 4 (150 mg, 1.64 mmol) was treated with octyl chloride(1.81 mmol, 0.3 mL) and TEA (0.4 mL) to give 267 mg (75%) of 5 as an amorphous white solid. 1H NMR(400 MHz, DMSO-d6) 7.40 (d, J = 8.1 Hz, 1H, NHCO), 4.55 (t, J = 5.5 Hz, 2H, OH), 3.69 (m, 1H, CHNH),3.37 (t, J = 5.6 Hz, 4H, CH2OH), 2.06 (t, J = 7.4 Hz, 2H, CH2CO), 1.46 (m, 2H, CH2), 1.22 (m, 8H, CH2),0.86 (t, J = 6.8 Hz, 3H, CH3).

According to the analysis of related databases, 534-03-2, the application of this compound in the production field has become more and more popular.

Reference:
Article; Jimenez, Aranza; Garcia, Pablo; De La Puente, Sofia; Madrona, Andres; Camarasa, Maria Jose; Perez-Perez, Maria-Jesus; Quintela, Jose-Carlos; Garcia-del Portillo, Francisco; San-Felix, Ana; Molecules; vol. 23; 7; (2018);,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Sep-21 News The origin of a common compound about 1072-52-2

With the rapid development of chemical substances, we look forward to future research findings about 1072-52-2.

The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 1072-52-2, name is 2-(Aziridin-1-yl)ethanol. This compound has unique chemical properties. The synthetic route is as follows. Product Details of 1072-52-2

Example 15 (Table 1, entry 8 and Scheme 11): Preparation of methyl 3-[(2-bromoethyl)- 2-[(methylsulfonyloxy)ethyl]amino]-2,6-dinitrobenzoate (27b); A solution of methyl 3- chloro-2,6-dinitrobenzoate (25) (1.15 g, 5.0 mmol) in dry DMF (10 mL) was treated with aziridineethanol (1.3 g, 15.0 mmol) and LiBr (4.35 g, 50 mmol)and stirred at room temperature for 6 h. The mixture was diluted with brine (40 mL) and extracted with EtOAc (2×60 mL). The combined organic fractions were washed with brine dried and concentrated under reduced pressure. Chromatography of the residue on silica gel, eluting with EtOAc/petroleum ether gave methyl 3-[(2-chloroethyl)(2-hydroxyethyl)amino]-2,6-dinitrobenzoate (26b) (0.40 g, 36% based on consumed starting material) as a yellow oil: 1H NMR [(CD3)2SO] delta 8.24 (d, / = 9.4 Hz, 1 H), 7.62 (dj = 9.4 Hz, 1 H), 4.79 (vbr s, 1 H), 3.78 (s, 3 H), 3.77 (t, / = 6.2 Hz, 2 H), 3.65 (t, / = 6.1 Hz, 2 H), 3.53 (t, / = 5.4 Hz, 2 H), 3.36 (t, / = 5.3 Hz, 2 H); 13C NMR delta163.2, 147.6, 136.4, 134.5, 128.1, 126.3, 121.9, 58.1, 53.8, 53.6, 52.5, 29.7. 38b: HRMS (FAB) calcd for C12H1579BrN3O7 [M+H]+ m/z 392.0093; found 392.0093.

With the rapid development of chemical substances, we look forward to future research findings about 1072-52-2.

Reference:
Patent; AUCKLAND UNISERVICES LIMITED; WO2008/30112; (2008); A1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

9/27/21 News A new synthetic route of 616-29-5

The synthetic route of 616-29-5 has been constantly updated, and we look forward to future research findings.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 616-29-5, name is 1,3-Diaminopropan-2-ol, the common compound, a new synthetic route is introduced below. COA of Formula: C3H10N2O

First a 30mL methanol solution of salicyldehyde (30 mmol,3.66 g) was added to a 15mL methanol solution of 1,3-diamino-2-propanol (15 mmol, 1.35 g). The resulting orange solution wasthen refluxed for 1 h, and after cooling down, the solvent wasremoved under reduced pressure to afford an orange crystallinesolid which was collected as the ligand. Yield: 69%. Anal. Calc. forC17H18N2O3: C, 68.42; H, 6.09; N, 9.39. Found: C, 68.77; H, 5.73; N,9.71%.

The synthetic route of 616-29-5 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Das, Kuheli; Massera, Chiara; Garribba, Eugenio; Frontera, Antonio; Datta, Amitabha; Journal of Molecular Structure; vol. 1199; (2020);,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts