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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076313Generated: October 26, 2026

Phenylacetone → 3-Phenyl-6-(m-chlorophenyl)-5-hexen-2-one

https://huagongshe.com/reaction/1076313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetoneHCID 7678—
ReactantSodium hydrideHCID 24758—
Reactantm-Chlorocinnamyl bromideHCID 54032824—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-Phenyl-6-(m-chlorophenyl)-5-hexen-2-oneHCID 53705377—

Reaction Steps

Sodium hydride (25.20 g., 0.60 mole, oil dispersion) is suspended in glyme (800 ml.) and phenyl acetone (80.50 g., 0.60 mole) in glyme (100 ml.) is added dropwise with stirring. After complete addition the mixture is heated to reflux for one hour. The mixture is cooled to room temperature and a solution of crude m-chlorocinnamyl bromide (139 g., 0.6 mole) in glyme (100 ml.) is added dropwise. When addition is complete the mixture is refluxed for 24 hours then allowed to cool. After filtration of inorganic salts and removal of solvent from the filtrate, vacuum distillation provides 36.11 g., b.p. 158.5°-163°/0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956374
Source datasetuspto-grants-1976_05
ORD IDord-84d02f43db0a4194a5d81565a0c94a27
Source noteuspto-grants-1976_05