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HRID 36900作成日:2026年10月26日

Ethanol → 3-Ethoxy-3-oxo-2-phenylpropanoic acid

https://huagongshe.com/reaction/36900

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Thionyl ChlorideHCID 24386—
反応物Phenylmalonic acidHCID 75791—
触媒DimethylformamideHCID 6228—
溶媒Diethyl EtherHCID 3283—
生成物3-Ethoxy-3-oxo-2-phenylpropanoic acidHCID 2729903—

反応手順

Phenylmalonic acid (13.5 g, 0.07 mol) in dry ether (40 mL) was treated with thionyl chloride (8.92 g, 5.4 mL, 0.07 mol) and one drop of N,N-dimethylformamide. 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), the solution was treated with ethanol (0.075 mol, 4.1 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 was 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05418244
出典データセットuspto-grants-1995_05
ORD IDord-d0d304e48bc64f40b143545cd4b9d69b
出典メモuspto-grants-1995_05