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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354589Generated: October 28, 2026

1-Chloro-4-(4-chlorophenyl)butan-2-ol → 1-Chloro-4-(4-chlorophenyl)butan-2-one

https://huagongshe.com/reaction/354589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(4-chlorophenyl)butan-2-olHCID 12432033—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-Chloro-4-(4-chlorophenyl)butan-2-oneHCID 1281646597.7%

Reaction Steps

A solution of 1-chloro-4-(4-chlorophenyl)-2-butanol (125 g) in acetone (200 ml) at 0° C. was treated with 570 ml of Jones reagent (from sodium dichromate dihydrate (100 g), concentrated sulfuric acid (136 g) and water to 500 ml) and stirred overnight at room temperature. The resulting solution was diluted with water (200 ml), extracted with ether (3×300 ml) and the extracts washed with water, aqueous sodium bicarbonate, and dried (MgSO4). Evaporation of the ether gave 121 g of 1-chloro-4-(4-chlorophenyl)-2-butanone. The analytical sample from hexane had m.p. 65°-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04375474
Source datasetuspto-grants-1983_03
ORD IDord-864bb812126e4cc4b9f770d7b72f7ab3
Source noteuspto-grants-1983_03