참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Butanedioic acid, 2-methyl-, 1,4-dimethyl ester | HCID 15350 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-(4-Chloro-benzylidene)-3-methyl-succinic acid | HCID 67304200 | 26.3% |
반응 단계
After careful addition of absolute methanol (0.1 mL) to a suspension of sodium hydride (60% in mineral oil, 16 g, 0.40 mol) in anhydrous toluene (200 mL), a solution of 4-chloro-benzaldehyde (28 g, 0.20 mol) and 2-methyl-succinic acid dimethyl ester (48 g, 0.30 mol) in anhydrous toluene (100 mL) was added dropwise at room temperature under a stream of nitrogen. After being stirred at room temperature for 2 hours, the resulting mixture was diluted by adding 2 N sodium hydroxide (200 mL) dropwise, then heated to 80° C., and stirred at the same temperature for 2 hours. After being cooled to room temperature naturally, the aqueous layer was separated, washed with ethyl acetate (100 mL×3), then acidified with 2 N hydrochloric acid to pH 2, and extracted with ethyl acetate (150 mL×3). The combined organic layers were dried over sodium sulfate, and concentrated in vacuo. The residue was precipitated from ethyl acetate/petroleum ether (10:1) to give 2-(4-chloro-benzylidene)-3-methyl-succinic acid (13.4 g, 26%) as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642629B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-a0f2adc394ca490f87771b901d954ca3 |
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| 출처 메모 | uspto-grants-2014_02 |
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