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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058393Generated: November 2, 2026

(E)-2-chloro-4-[3-(3-hydroxyphenyl)-1-oxoprop-2-en-1-yl]benzoic acid methyl ester → 2-Chloro-4-[1-oxo-3-(3-hydroxyphenyl)propyl]benzoic acid, methyl ester

https://huagongshe.com/reaction/1058393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-2-chloro-4-[3-(3-hydroxyphenyl)-1-oxoprop-2-en-1-yl]benzoic acid methyl esterHCID 23560779—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-4-[1-hydroxy-3-(3-hydroxyphenyl)propyl]benzoic acid, methyl esterHCID 2356077826%
Product2-Chloro-4-[1-oxo-3-(3-hydroxyphenyl)propyl]benzoic acid, methyl esterHCID 2356078064%

Reaction Steps

A mixture (E)-2-chloro-4-[3-(3-hydroxyphenyl)-1-oxoprop-2-en-1-yl]benzoic acid methyl ester (Example 91; 250 mg, 0.8 mmol) and 10% palladium-on-charcoal (25 mg) in ethyl acetate (5 mL) was hydrogenated at atmospheric pressure for 90 min. The reaction mixture was filtered through Celite® and the filter cake was washed with ethyl acetate. The solvent was evaporated under reduced pressure and the residue was then chromatographed over silica gel (20-50% ethyl acetate/hexanes) to give 2-chloro-4-[3-(3-hydroxyphenyl)-1-oxopropan-1-yl]benzoic acid, methyl ester (160 mg, 64% yield) and rac.-2-chloro-4-[1-hydroxy-3-(3-hydroxyphenyl)propan-1-yl]benzoic acid, methyl ester (65 mg, 26% yield). The alcohol was obtained as a racemic mixture and was not resolved.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515124B2
Source datasetuspto-grants-2003_02
ORD IDord-3febfeed252543ef902356fd5d00b4af
Source noteuspto-grants-2003_02