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HRID 1683189作成日:2026年10月27日

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

https://huagongshe.com/reaction/1683189

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US05637601
出典データセットuspto-grants-1997_06
ORD IDord-3485aa26f5ab4dec88797a654057632a
出典メモuspto-grants-1997_06