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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133792생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/133792

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참여 물질

역할이름HCID투입량
반응물Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 76150—
반응물Sodium borohydrideHCID 4311764—
촉매Sodium SulfateHCID 24436—
용매MethanolHCID 887—
생성물Ethyl 3-hydroxy-3-(4-methoxyphenyl)propanoateHCID 1109623256.2%

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온도0 °C

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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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390925B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-8116151a36d54ab390cb89a4201515d4
출처 메모uspto-grants-2008_06