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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52864Generated: October 26, 2026

3,4-Dichlorobenzyl chloride → 4-(3,4-Dichlorophenyl)-3-(2-fluoro-4-biphenylyl)-2-butanone

https://huagongshe.com/reaction/52864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantSodium HydroxideHCID 14798—
Reactant2-Fluoro-4-biphenylyl acetoneHCID 12950418—
Product4-(3,4-Dichlorophenyl)-3-(2-fluoro-4-biphenylyl)-2-butanoneHCID 1907361385%

Reaction Conditions

Temperature100 °C

Reaction Steps

45.1 g of the ketone compound thus obtained, 50.3 g of 3,4-dichlorobenzyl chloride and 15.8 g of sodium hydroxide were mixed, heated with stirring at 100° C. for 6 hours. The reaction solution was left to cool to room temperature and then extracted by an addition of ethyl acetate and water. The organic layer was post-treated by a conventional method. Then, the product was purified by silica gel column chromatography (hexane/ethyl acetate=50/1) to obtain 65.0 g (yield: 85%) of 4-(3,4-dichlorophenyl)-3-(2-fluoro-4-biphenylyl)-2-butanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616803
Source datasetuspto-grants-1997_04
ORD IDord-1add2f6c5621410ab3b61f86e55ce5fc
Source noteuspto-grants-1997_04