Month: August 2021

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 4442-79-9, name is 2-Cyclohexylethanol. A new synthetic method of this compound is introduced below., category: alcohols-buliding-blocks

150 mg (1.17 mmol, 1 eq) of 2-cyclohexylethanol were diluted in 4 mL of DCM, 214 muL (1.52 mmol, 1.3 eq) of triethylamine were added. The mixture was cooled to 0C and 100 muL (1.29 mmol, 1.1 eq) of mesyl chloride were added. The mixture was stirred for 15 min at 00C then water was added. The aqueous phase was extracted with dichloromethane. The organic phase was washed with water, brine, dried over MgSO4, filtered and concentrated in vacuo. The crude product (241 mg) was used directly for synthesis of 2. TLC : Rf : 0.48 (eluant : Heptane/EtOAc : 1/1).

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 4442-79-9, 2-Cyclohexylethanol.

Reference:
Patent; AMGEN INC.; WO2009/9122; (2009); A2;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

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. 27489-62-9, name is trans-4-Aminocyclohexanol, the common compound, a new synthetic route is introduced below. Product Details of 27489-62-9

A mixture of Methyl 2-bromo-1 -methyl-1 H-benzimidazoIe-5-carboxylate (37.0 g, 0.137 mol), frans-4-aminocyclohexanol (38.0 g, 0.33 mol), cesium fluoride CsF (29.24 g, 0.29 mol), and DMSO (350 mL) was stirred at 110 C for 6 h and kept overnight at room temperature (TLC control, silica gel, chloroform/ethanol 20:1 ). The reaction mixture was poured into cold water (1.5 L). The precipitate was separated by filtration and recrystallized from acetonitrile (900 mL) to give the title compound in 84% (35.0 g) yield.

The synthetic route of 27489-62-9 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; PFIZER PRODUCTS INC.; WO2007/69053; (2007); A1;,
Alcohol – Wikipedia,
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Application of 440-60-8, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 440-60-8, name is (Perfluorophenyl)methanol. A new synthetic method of this compound is introduced below.

Example 10 In a 30 ml two-necked flask were added 0.004 g of LiOH.H2O, 0.31 g of methyl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate, 1.00 g of (2,3,4,5,6-pentafluorophenyl)methyl alcohol and 0.6 g of toluene, and the mixture was stirred for 8 hours at a toluene refluxing temperature. Analysis of the reaction mixture by a gas chromatography showed that the yield of (2,3,4,5,6-pentafluorophenyl)methyl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate was 92% based on the starting ester.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,440-60-8, (Perfluorophenyl)methanol, and friends who are interested can also refer to it.

Reference:
Patent; Sumitomo Chemical Company, Limited; US6441220; (2002); B1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Related Products of 5333-42-6, 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 5333-42-6, name is 2-octyldodecan-1-ol. This compound has unique chemical properties. The synthetic route is as follows.

2-Octyl-l-dodecanol (5 g, 16.7 mmol) was taken in a 100 mL round bottomed flask, pyridiniumchlorochromate (10.8 g, 50.24 mmol) was added to it and the mixture was dissolved in anhydrous CH2C12 (120 mL). The reaction mixture was stirred at room temperature (27C) for 3 h and filtered through a short pad of silica gel to provide the required aldehyde as a colourless liquid. 4.68 g, Yield: 94%.1H NMR (400 MHz, CDC13) delta: 9.54 (d, / = 3.2 Hz, 1 H), 2.26 – 2.14 (m, 1 H), 1.68 – 1.53 (m, 2 H), 1.42 (dd, / = 14.2, 5.6 Hz, 2 H), 1.25 (broad s, 28 H), 0.87 (t, / = 6.8 Hz, 6 H); 13C NMR (100 MHz, CDC13) delta: 211.9, 182.8, 161.1, 77.3, 77.2, 76.7, 74.6, 72.1, 45.5, 42.8, 37.4, 34.0, 32.2, 31.9, 31.8, 29.7, (0101) 29.6, 29.6, 29.5, 29.5, 29.3, 29.3, 29.3, 29.1, 27.4, 25.6, 25.2, 23.9, 22.7, 14.1; MALDI-TOF (m/z): [M]+ calcd for C20H40O: 296.3079; found: 296.2517.

According to the analysis of related databases, 5333-42-6, the application of this compound in the production field has become more and more popular.

Reference:
Patent; COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH; NITHYANANDAN, Jayaraj; ALAGUMALAI, Ananthan; FAIROOS, Munavvar; VELLIMALAI, Punitharasu; (47 pag.)WO2018/20518; (2018); A1;,
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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 1202577-61-4, name is trans-(4-(Trifluoromethyl)cyclohexyl)methanol. This compound has unique chemical properties. The synthetic route is as follows. Quality Control of trans-(4-(Trifluoromethyl)cyclohexyl)methanol

[00173] To a mixture of oxalyl chloride (24.96 g, 13.84 mL, 197.7 mmol) in CH2C12 (250 mL) was added dropwise DMSO (20.72 g, 28 mL, 395.4 mmol) at -65 C. The mixture was stirred at -65 C for 30 min. (iraw5,-4-(trifluoromethyl)cyclohexyl)methanol (12 g, 65.9 mmol) dissolved in CH2C12 (50 mL) was added dropwise at -65 C and the mixture was stirred at -65 C for another 30 min. Triethylamine (66.4 g, 91.2 mL, 659 mmol) was added dropwise below -65 C. The mixture was stirred at -65 C for 30 min, then stirred at rt for 1.5 h. The mixture was quenched with water (200 mL) and separated. The aqueous layer was extracted with CH2C12 (2 x 300 mL). The combined organic layers were washed with water (200 mL) and brine (200 mL), dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. The residue was purified by silica gel chromatography (eluting with petroleum ether: ethyl acetate = 10: 1) to give trans-4- (trifluoromethyl)cyclohexanecarbaldehyde (8.9 g, 75%) as a slight yellow oil. 1H NMR (CDCI3, 400 MHz): delta 9.70 (s, 1H), 2.16-2.65 (m, 3H), 2.04-2.12 (m, 3H), 1.00-1.39 (m, 4H).

With the rapid development of chemical substances, we look forward to future research findings about 1202577-61-4.

Reference:
Patent; VITAE PHARMACEUTICALS, INC.; CLAREMON, David, A.; DILLARD, Lawrence, Wayne; DONG, Chengguo; FAN, Yi; JIA, Lanqi; LOTESTA, Stephen, D.; MARCUS, Andrew; SINGH, Suresh, B.; TICE, Colin, M.; YUAN, Jing; ZHAO, Wei; ZHENG, Yajun; ZHUANG, Linghang; (102 pag.)WO2016/61160; (2016); A1;,
Alcohol – Wikipedia,
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Synthetic Route of 110-73-6, 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 110-73-6, name is 2-(Ethylamino)ethanol. This compound has unique chemical properties. The synthetic route is as follows.

in a four-necked flask of 300ml, formula dye intermediate 34.3 parts obtained in step 5-1, put the NMP146 parts of 2- (ethylamino) ethanol 16.3 parts, 90 in it stirred 1.5 hours.The reaction mixture was poured into 2N aqueous hydrochloric acid, the precipitated crystals were collected by filtration, washed, and dried to give Intermediate 34.9 parts of the dye represented by the following formula (104).

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 110-73-6, 2-(Ethylamino)ethanol.

Reference:
Patent; NIPPON KAYAKU COMPANY LIMITED; MIFUJI, AKIHIRO; (16 pag.)JP2016/65220; (2016); A;,
Alcohol – Wikipedia,
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Electric Literature of 5339-85-5, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 5339-85-5 as follows.

The conversion of 2-(o-aminophenyl)ethanol and the yield of indole were 100% and 91.6%, respectively.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,5339-85-5, its application will become more common.

Reference:
Patent; Research Association for Utilization of Light Oil; US4757152; (1988); A;,
Alcohol – Wikipedia,
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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 403-41-8, name is 1-(4-Fluorophenyl)ethyl Alcohol. This compound has unique chemical properties. The synthetic route is as follows. category: alcohols-buliding-blocks

To a solution of 1-(4-fluorophenyl)ethanol (200 mg, 0.0014 mol, commercial source: Aochem) in dichloromethane (4 mL), triethylamine (0.4 mL, 0.0029 mol, commercial source: Finar) and mesyl chloride (0.16 mL, 0.0021 mol, commercial source: Avra) were added at 0 C. The reaction mixture was stirred at 26 C for 16 h. Upon completion, dichloromethane (60 mL) and water (10 mL) were added. The organic layer was dried over anhydrous Na2S04, filtered and the filtrate was concentrated under reduced pressure to afford crude 1-(4-fluorophenyl)ethyl methanesulfonate (300 mg) as a pale tellow liquid that was used in the next step without further purification.

With the rapid development of chemical substances, we look forward to future research findings about 403-41-8.

Reference:
Patent; GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED; ALEMPARTE-GALLARDO, Carlos; ENCINAS, Lourdes; ESQUIVIAS PROVENCIO, Jorge; (206 pag.)WO2019/34729; (2019); A1;,
Alcohol – Wikipedia,
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Related Products of 29683-23-6, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 29683-23-6, name is Tetrahydro-2H-thiopyran-4-ol, molecular formula is C5H10OS, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

Phosphorus tribromide (3.9 g, 14 mmol) was added dropwise in 30 min to a solution of alcohol 5 (3.73 g, 32 mmol) in CH2Cl2 (50 mL) at ambient temperature. Upon completion of the addition, the reaction mixture was slowly heated to the boiling point and stirred overnight. After cooling to room temperature the mixture was quenched with water and extracted with diethyl ether (2 × 100 mL). The organic phase was washed with a saturated solution of NaHCO3, dried over anhydrous MgSO4 and evaporated to yield 3.37 g (19 mmol, 59%) of a yellow oil. deltaH (CDCl3) 4.32 (m, 1H, CHBr), 2.90 (m, 2H, SCH2), 2.55 (m, 2H, SCH2), 2.38 (m, 2H, SCH2CH2), 2.23 (m, 2H, SCH2CH2). deltaC (CDCl3) 45.3 (CBr), 36.9 (SCC), 26.9 (SC).

According to the analysis of related databases, 29683-23-6, the application of this compound in the production field has become more and more popular.

Reference:
Article; Van Walree, Cornelis A.; Lutz, Martin; Spek, Anthony L.; Jenneskens, Leonardus W.; Havenith, Remco W.A.; Journal of Molecular Structure; vol. 1036; (2013); p. 115 – 120;,
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Related Products of 2240-88-2, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 2240-88-2 as follows.

b) Methyl 4-(benzyloxy)-3-(3,3,3-trifluoropropoxy)benzoateDiisopropyl azodicarboxylate (0.372 mL, 1.89 mmol) and triphenylphosphine (0.489 g, 1.86 mmol) were added to a solution of methyl 4-(benzyloxy)-3-hydroxybenzoate (0.355 g, 1.37 mmol) in tetrahydrofuran (20 mL) and the resulting reaction mixture was stirred for 55 min at room temperature. 3,3,3-Trifluoro-l-propanol (0.121 mL, 1.37 mmol) was added and the reaction mixture was stirred over night. The solvent was evaporated. Purification by column chromatography, using heptane/ethyl acetate (6:1) as the eluent, gave 0.162 g (33percent yield) of the title compound. GC MS (EI) m/z 354 [M]+*.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,2240-88-2, its application will become more common.

Reference:
Patent; ASTRAZENECA AB; BYLUND, Johan; EK, Maria, E; HOLENZ, Joerg; KERS, Annika; OeHBERG, Liselotte; WO2010/132016; (2010); A1;,
Alcohol – Wikipedia,
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