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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607210Generated: October 30, 2026

Acetone → 1-(3,4-Dichlorophenyl)-2-phenylethanone

https://huagongshe.com/reaction/1607210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSulfuric AcidHCID 1118—
Reactant3,4-Dichlorophenyl benzyl carbinolHCID 19852792—
SolventWaterHCID 962—
Product1-(3,4-Dichlorophenyl)-2-phenylethanoneHCID 2758145—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 500 ml round bottomed flask was placed 75 g of crude 3,4-dichlorophenyl benzyl carbinol and 300 ml of acetone. The reaction mixture was cooled to 0° C. and a solution of 20 g of chromic anhydride and 17.25 ml of concentrated sulfuric acid in 60 ml of water was added at a rate to keep the internal temperature below 5° C. After stirring an additional 15 minutes, the reaction was quenched with 10 ml of isopropanol and partitioned between ethyl ether and water. The organic layer was washed with brine, dried, and concentrated. The resulting crude ketone was crystallized from hexane yielding 51 g of 3,4-dichlorophenyl benzyl ketone. NMR data was consistent with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863947
Source datasetuspto-grants-1989_09
ORD IDord-f1ab14c89bb244719691a29507a292ca
Source noteuspto-grants-1989_09