Sources of common compounds: 186020-66-6

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Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 186020-66-6, name is tert-Butyl 12-Hydroxy-4,7,10-trioxadodecanoate. This compound has unique chemical properties. The synthetic route is as follows. HPLC of Formula: C13H26O6

3,6,9-Trioxadodecan-12-oic acid, l-[[3-trifluoromethyl-7-oxa-bicyclo[2.2.1]hepta-2,5- diene-2-carboxyl]oxy]-l,l-dimethylethyl ester (10); A mixture of 5 (103 mg, 0.50 mmol), tert-butyl-12-hydroxy-4,7,10-trioxadodecanoate (139 mg, 0.50 mmol) and 4-(dimethylamino)-pyridine (DMAP, 121 mg, 1.00 mmol) in CH2Cl2 (6 mL) was cooled to 0 0C before adding l-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDCHCl, 105 mg, 0.55 mmol). The mixture was stirred for 5 min. at 0 0C and 18 hours at room temperature. The reaction mixture was acidified with HCl (2M) to a pH of 1-2 and extracted with CH2Cl2 (2 x 10 mL). The combined organic layers were dried over MgSO4 and concentrated in vacuo. The crude mixture was purified by preparative TLC (CH2Cl2/Me0H, 9/1) resulting in compound 10 as a slightly yellow oil (65 mg (27%)). Rf= 0.81 (CH2Cl2/Me0H, 9/1). 1H-NMR (400 MHz, CDCl3) delta (ppm): 7.19 (dd, J = 5.3, 1.9 Hz, IH), 7.29 (dd, J = 5.3, 1.9 Hz, IH), 5.71 (dd, J = 2.9, 1.6 Hz, IH), 5.66 (t, J = 1.7 Hz, IH), 4.36 (ddt, J = 11.9, 11.9, 7.1, 4.9 Hz, 2H), 3.73 (t, J = 4.9, 2H), 3.70 (t, J = 6.6 Hz, 2H), 3.64 (s, 6H), 3.60 (m, 2H), 2.49 (t, J= 6.6 Hz, 2H), 1.44 (s, 9H). LCQ MS(ESI+) m/z (%) 489.0 (50) [M+Na]+, 410.9 (50) [M-(CH3)2C=C]+

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, 186020-66-6, tert-Butyl 12-Hydroxy-4,7,10-trioxadodecanoate.

Reference:
Patent; STICHTING VOOR DE TECHNISCHE WETENSCHAPPEN; STICHTING KATHOLIEKE UNIVERSITEIT NIJMEGEN; WO2008/75955; (2008); A2;,
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