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HRID 36901作成日:2026年10月23日

Methanol → 3-Methoxy-3-oxo-2-phenylpropanoic acid

https://huagongshe.com/ja/reaction/36901

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
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-Methoxy-3-oxo-2-phenylpropanoic acidHCID 2817775—

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, 0.071 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.

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-12d7ef5cb8464e28908246b96bdc2ed8
出典メモuspto-grants-1995_05