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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 467150생성일: 2026년 10월 24일

Triethylamine → 4-p-methoxyphenylbutyryl-L-prolinal dimethyl acetal

https://huagongshe.com/ko/reaction/467150

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(4-Methoxyphenyl)butyric acidHCID 78280—
반응물DiethylphosphorylcyanideHCID 13586794—
반응물Benzene ethyl acetateHCID 21583983—
용매DimethylformamideHCID 6228—
생성물4-p-methoxyphenylbutyryl-L-prolinal dimethyl acetalHCID 1513263958%

반응 단계

L-prolinal dimethyl acetal hydrochloride obtained in the same manner as in Example 1 is dissolved in dimethylformamide (4 ml) containing 4-p-methoxyphenylbutyric acid (740 mg, 3.81 mmol) and diethylphosphoryl cyanide (0.48 ml, 3.16 mmol). To the solution is added dropwise triethylamine (1.15 ml, 8.25 mmol) under cooling and agitation in an ice-methanol bath. After the dropwise addition, the mixture is continued to be stirred for one hour under cooling and then for one hour at room temperature. Benzene-ethyl acetate (2:1, 150 ml) is added to the reaction mixture, and the organic layer is separated, washed successively with a saturated aqueous solution of sodium hydrogen carbonate (15 ml), water (15 ml) and a saturated aqueous solution of edible salt (15 ml), dried over sodium sulfate and filtered. The filtrate is concentrated to dryness under reduced pressure. The residue is purified by column chromatography on silica gel (benzene-ethyl acetate, 1:2→1:1) to give 727 mg (58%) of the title compound as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05158970
출처 데이터셋uspto-grants-1992_10
ORD IDord-be129163bb1b45f48b3bb23d755404ea
출처 메모uspto-grants-1992_10