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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344932Generated: October 29, 2026

Chloroacetyl chloride → 2-Chloroacetyl-4-(5-ethyl-2-methoxyphenyl)phenol

https://huagongshe.com/reaction/344932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Ethyl-2,4'-dimethoxybiphenylHCID 54184217—
Solvent1,2-DichloroethaneHCID 11—
Product2-Chloroacetyl-4-(5-ethyl-2-methoxyphenyl)phenolHCID 54455371—

Reaction Steps

A mixture was prepared by suspending 25 g of aluminium chloride into 100 ml of 1,2-dichloroethane. The mixture, wherein 5 ml chloroacetyl chloride was added, was stirred for 1 hour at room temperature, followed by dropwise addition of 5-ethyl-2,4'-dimethoxy-biphenyl, wherein 10 g of 1.2-dichloroethane was dropwise and stirred overnight at room temperature. The reaction mixture was transferred into ice water to extract with dichloroethane. The extract was washed with saturated salt water, dried with sodium sulfate and concentrated. The concentrate was purified by a silica gel column chromatography (10:1, n-hexane:ethyl acetate) and recrystallized from chloroform/n-hexane to yield 2.5 g of light yellow and powdered 2-chloroacetyl-4-(5-ethyl-2-methoxyphenyl)phenol having a m.p. of 67.0°-68.0° C. Then, the fraction which was eluted with n-hexane/ethyl acetate: 3/1, was concentrated. The concentrate was recrystallized from chloroform/n-hexane to yield 1.5 g of white powder 3,3-bischloroacetyl-5-ethyl-2,4'-biphenyldiol having a m.p. of 154.0°-155.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053548
Source datasetuspto-grants-1991_10
ORD IDord-c1350cb312864b1f8bb82d3a38d06fab
Source noteuspto-grants-1991_10