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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133792Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/133792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl esterHCID 76150—
EduktSodium borohydrideHCID 4311764—
KatalysatorSodium SulfateHCID 24436—
LösungsmittelMethanolHCID 887—
ProduktEthyl 3-hydroxy-3-(4-methoxyphenyl)propanoateHCID 1109623256,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390925B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-8116151a36d54ab390cb89a4201515d4
Quellennotizuspto-grants-2008_06