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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587583Generated: November 1, 2026

Ethanol → alpha-Methyl-4'-(hydroxy)[1,1'-biphenyl]-4-acetic acid, ethyl ester

https://huagongshe.com/reaction/1587583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactantalpha-Methyl-4'-(hydroxy)[1,1'-biphenyl]-4-acetic acidHCID 18956586—
SolventSulfuric AcidHCID 1118—
Productalpha-Methyl-4'-(hydroxy)[1,1'-biphenyl]-4-acetic acid, ethyl esterHCID 8674694273.5%

Reaction Steps

A mixture of α-methyl-4'-(hydroxy)[1,1'-biphenyl]-4-acetic acid (22.0 g, 90.8 mmol) in ethanol (500 mL) and concentrated sulfuric acid (5.0 mL) is refluxed for 30 hours. The solution is concentrated under reduced pressure, is diluted with water (300 mL) and is extracted with ethyl acetate (3×300 mL). The combined ethyl acetate extract is washed with water (400 mL) and brine (400 mL), dried over MgSO4 and is concentrated under reduced pressure to give 20 g of crude product. Purification of this material by column chromatography (25% ethyl acetate in hexane) followed by crystallization from ethyl acetate and hexane gives 18.0 g (73.5%) of crystalline product, m.p. 124°-125° C., MS(CI+ m/z): 271[M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05218124
Source datasetuspto-grants-1993_06
ORD IDord-0f37ba6fb38f4b978394dc4bba69336c
Source noteuspto-grants-1993_06