참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-(4-Methoxyphenyl)butyric acid | HCID 78280 | — |
| 반응물 | Diethylphosphorylcyanide | HCID 13586794 | — |
| 반응물 | Benzene ethyl acetate | HCID 21583983 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-p-methoxyphenylbutyryl-L-prolinal dimethyl acetal | HCID 15132639 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05158970 |
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| 출처 데이터셋 | uspto-grants-1992_10 |
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| ORD ID | ord-be129163bb1b45f48b3bb23d755404ea |
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| 출처 메모 | uspto-grants-1992_10 |
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