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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058391Generated: November 2, 2026

Acetone → Rac.-(e)-2-chloro-4-[1-hydroxy-3-(3-hydroxyphenyl)prop-2-en-1-yl]benzoic acid methyl ester

https://huagongshe.com/reaction/1058391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-2-chloro-4-[3-(3-hydroxyphenyl)-1-oxoprop-2-en-1-yl]benzoic acid methyl esterHCID 23560779—
SolventMethanolHCID 887—
ProductRac.-(e)-2-chloro-4-[1-hydroxy-3-(3-hydroxyphenyl)prop-2-en-1-yl]benzoic acid methyl esterHCID 2356077797.3%

Reaction Steps

Sodium borohydride (25 mg, 0.66 mmol) was added to a solution of (E)-2-chloro-4-[3-(3-hydroxyphenyl)-1-oxoprop-2-en-1-yl]benzoic acid methyl ester (Example 91; 316 mg, 1 mmol) in methanol (3 mL). The solution was stirred at room temperature for 3 h, then acetone (1 mL) was added and the solution was stirred for a further 10 min. The solvent was evaporated, ethyl acetate (15 mL) was added and the solution was washed with 0.5N hydrochloric acid solution (10 mL) and brine. Each of the aqueous layers was extracted in turn with ethyl acetate (10 mL). The combined organic layers were dried (MgSO4), filtered, evaporated and the resulting solid was triturated with diethyl ether to furnish rac.-(E)-2-chloro-4-[1-hydroxy-3-(3-hydroxyphenyl)prop-2-en-1-yl]benzoic acid methyl ester (310 mg, 97% yield) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515124B2
Source datasetuspto-grants-2003_02
ORD IDord-90f5dfbb0bac463badd3a6a306c18e3d
Source noteuspto-grants-2003_02