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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582348Generated: October 25, 2026

Benzoyl chloride → 4-Benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene

https://huagongshe.com/reaction/582348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-Benzyloxy-3-chloro-5-methylphenolHCID 18504631—
SolventChloroformHCID 6212—
Product4-Benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzeneHCID 1850455490.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 27.3 g of 4-benzyloxy-3-chloro-5-methylphenol dissolved in 250 ml of chloroform and being stirred at 0° C. were added 15.4 g of benzoyl chloride and then 13.3 g of triethylamine. After stirring at room temperature for 2 hours, the chloroform layer was washed with water, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel chromatography, which afforded 35 g of 4-benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene (90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922880
Source datasetuspto-grants-1999_07
ORD IDord-9ab2cc95132849719f007229ed560d57
Source noteuspto-grants-1999_07