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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416369Generated: October 25, 2026

1-(2,3-Dichlorophenyl)ethanol → 1-(2,3-Dichlorophenyl)ethan-1-one

https://huagongshe.com/reaction/1416369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,3-Dichlorophenyl)ethanolHCID 600228—
ReactantSodium HypochloriteHCID 23665760—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetic AcidHCID 176—
Product1-(2,3-Dichlorophenyl)ethan-1-oneHCID 9198665%

Reaction Conditions

Temperature20 °C

Reaction Steps

α-Methyl-2,3-dichlorobenzyl alcohol (5.0 g, 0.026 mol was dissolved in acetic acid (24 ml) and 12% w/v sodium hypochlorite solution (23.26 ml, 0.0314 mol) was added slowly dropwise, with stirring, at a temperature of 15-25° C. When the addition was complete the reaction mixture was stirred at ambient temperature for approximately 11/2 hours until a starch/iodide test gave a positive result. Saturated sodium bisulphite solution was added to the reaction mixture until the starch/iodide test was negative. The mixture was poured onto ice/brine (100 ml) and extracted with diethyl ether (3×75 ml). The ether phases were combined and washed with 2N sodium hydroxide solution (3×75 ml) until the aqueous washes were alkaline. The ether phase was dried over anhydrous magnesium sulphate, filtered and evaporated down. 2,3-Dichloroacetophenone (3.2 g, 65% yield) was afforded as a pale-yellow oil. T.l.c. (SiO2 ;CHCl3) and nmr showed this material to contain no impurities.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912345
Source datasetuspto-grants-1999_06
ORD IDord-937f85b3d7e34ef1a2c2897c62ae291c
Source noteuspto-grants-1999_06