成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

429-01-6

6-METHYL-2,4,6-TRIS(TRIFLUOROMETHYL)TETRAHYDROPYRAN-2,4-DIOL synthesis

3synthesis methods
-

Yield:429-01-6 73%

Reaction Conditions:

with potassium tert-butylate in tetrahydrofuran at 20; for 4 h;

Steps:

E 1 preparation of 4,6-dihydroxy-2-methyl-2,4,6-tris(trifluoromethyl)-tetrahydropyran

n a 500 ML three-neck round bottom flask equipped with a teflon stirrer, a thermocouple and a nitrogen inlet, 88 ML of a 1 M THF solution of potassium tert-butoxide were cooled to a temperature ranging from -30° to -50°C. A 40 ML quantity of trifluoroacetone was slowly added to the flask to form a reaction mixture and the reaction mixture was allowed to warm up to room temperature.. After four hours, the reaction mixture was poured onto a dilute solution of hydrochloric acid and the aqueous layer was extracted with ethyl ether.. The combined organic layers were dried and filtered and the solvent was evaporated to provide 36 grams of a white solid product after recrystallization from a hexane solvent.. The percentage yield of the product was 73%.. An analysis of the product identified it as 4,6-dihydroxy-2-methyl-2,4,6-tris(trifluoromethyl)-tetrahydropyran (four stereoisomers, one major).. The mass spectrum and NMR results for the product were as follows: mass spectrum m/z (267, M - CF3), 1H NMR of the major component (CD3OD, ppm) 4.86 (s, 2H), 1.79 (s, 3H), 1.84 - 186 (d, 1 H), 1.91 -1.94 (d, 1 H), 1.97 -2.00 (d, 1 H), 2.1 - 2.17 (d, 1 H); 19F NMR of the major component (CD3OD, ppm) -89.2 (s, CF3), -87.3 (s, CF3), -87.1 (s, CF3).

References:

EP1449839,2004,A2 Location in patent:Page 9

6-METHYL-2,4,6-TRIS(TRIFLUOROMETHYL)TETRAHYDROPYRAN-2,4-DIOL Related Search: