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HRID 5621作成日:2026年10月23日

Trifluoromethanesulfonic acid → Methyl (3R)-3-(benzyloxy)tetradecanoate

https://huagongshe.com/ja/reaction/5621

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoromethanesulfonic acidHCID 62406—
反応物Benzyl 2,2,2-trichloroacetimidateHCID 144968—
反応物3R-hydroxymyristic acid methyl esterHCID 9834945—
溶媒CyclohexaneHCID 8078—
生成物Methyl (3R)-3-(benzyloxy)tetradecanoateHCID 13817922112.8%

反応手順

A suspension of 206.7 g of methyl (R)-3-hydroxytetradecanoate in 1000 ml of cyclohexane was treated under nitrogen and while stirring with 214.2 g of benzyl trichloroacetimidate and dissolved at 20°. 10 ml of trifluoromethanesulphonic acid were added dropwise while cooling in an ice/water bath in such a manner that the temperature remains between 20°-23°. The resulting suspension was stirred at 25°-30°. The precipitate was filtered off, the filter cake was washed with cyclohexane, the filtrates were extracted with sat. NaHCO3 solution, water and sat. NaCl solution. The organic phase was dried over magnesium sulphate, filtered, the filter cake was washed with cyclohexane and the filtrates were evaporated. 314.5 g of methyl (R)-3-(benzyloxy)-tetradecanoate were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05245056
出典データセットuspto-grants-1993_09
ORD IDord-7aa6ea05ad5f4e639b91d1a44ecf298b
出典メモuspto-grants-1993_09