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HRID 467150作成日:2026年10月25日

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

https://huagongshe.com/reaction/467150

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-(4-Methoxyphenyl)butyric acidHCID 78280—
反応物DiethylphosphorylcyanideHCID 13586794—
反応物Benzene ethyl acetateHCID 21583983—
溶媒DimethylformamideHCID 6228—
生成物4-p-methoxyphenylbutyryl-L-prolinal dimethyl acetalHCID 1513263958%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05158970
出典データセットuspto-grants-1992_10
ORD IDord-be129163bb1b45f48b3bb23d755404ea
出典メモuspto-grants-1992_10