참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | Phenylmalonic acid | HCID 75791 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 3-Methoxy-3-oxo-2-phenylpropanoic acid | HCID 2817775 | — |
반응 단계
Phenylmalonic acid (13.5 g, 0.07 mol ) in dry ether (40 mL) was treated with thionyl chloride (8.92 g, 5.4 mL, 0.071 mol) and one drop of N,N-dimethyl formamide. The mixture was heated at 40°-50° C. for 3 hours. The clear solution was evaporated under reduced pressure to remove any residual thionyl chloride. The oily residue was redissolved in dry ether (40 mL) and the solution was treated with methyl alcohol (0.075 mol, 3 mL ) and refluxed for 2 hours. The reaction mixture was cooled to room temperature and washed with water. The organic layer was extracted with saturated solution of sodium bicarbonate until alkaline. The combined extracts were washed with ether and the aqueous layer acidified with 5N HCl to pH 1. The precipitated oil was extracted with CH2Cl2 (50 mL×3). The combined extracts were washed with water (50 mL×4) and dried over anhydrous MgSO4. The oily product crystallized on standing.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05418244 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-12d7ef5cb8464e28908246b96bdc2ed8 |
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| 출처 메모 | uspto-grants-1995_05 |
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