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HRID 133792作成日:2026年10月27日

Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester → Ethyl 3-hydroxy-3-(4-methoxyphenyl)propanoate

https://huagongshe.com/reaction/133792

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 76150—
反応物Sodium borohydrideHCID 4311764—
触媒Sodium SulfateHCID 24436—
溶媒MethanolHCID 887—
生成物Ethyl 3-hydroxy-3-(4-methoxyphenyl)propanoateHCID 1109623256.2%

反応条件

温度0 °C

反応手順

A solution of ethyl 3-(4-methoxyphenyl)-3-oxopropanoate (444 mg, 2 mmol) in methanol (4 mL) was added sodium borohydride (76 mg, 2.0 mmol) at 0° C. slowly. After addition, the reaction mixture was stirred at 0° C. for 30 min. Two drops of saturated sodium sulfate solution were added to the reaction mixture to quench the reaction. Methanol was removed in vacuo, and water was added to the residue. The aqueous solution was extrated with ethyl acetate (x3), and the combined organic layers were dried over anhydrous sodium sulfate, and filtered. The filtrate was evaporated in vacuo. The crude mixture was purified by Flash Chromatography with eluent of 40% ethyl acetate/60% hexane to give the title compound as a clear oil (252 mg, 56% yield). 1H NMR (400 MHz, CDCl3) δ 1.22-1.28 (m, 3 H) 2.63-2.75 (m, 2 H) 3.79 (s, 3 H) 4.16 (q, J=7.13 Hz, 2 H) 5.07 (dd, J=9.06, 3.78 Hz, 1 H) 6.85-6.89 (m, 2 H) 7.24-7.31 (m, 2 H). HPLC retention time: 1.973 min (method A). MS (ESI) (M+Na)+ 246.96.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390925B2
出典データセットuspto-grants-2008_06
ORD IDord-8116151a36d54ab390cb89a4201515d4
出典メモuspto-grants-2008_06