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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121841Generated: November 1, 2026

Bromoacetyl bromide → Ethyl 2-[4-(2-bromoacetyl)-3-chlorophenoxy]-2-methylpropionate

https://huagongshe.com/reaction/2121841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantEthyl 2-(3-chlorophenoxy)-2-methylpropanoateHCID 1531499—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 2-[4-(2-bromoacetyl)-3-chlorophenoxy]-2-methylpropionateHCID 15453491—

Reaction Steps

To a stirred suspension of aluminum chloride (1.8 g) in 1,2-dichloroethane (25 ml) was added bromoacetyl bromide (400 μl) under ice-cooling, and the mixture was stirred for 30 minutes. To the stirred mixture was added dropwise a solution of ethyl 2-(3-chlorophenoxy)-2-methylpropionate (1.1 g) in 1,2-dichloroethane (5 ml) under ice-cooling, and the mixture was stirred for 3 hours at 60° C. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Purification of the residue by flash column chromatography on silica gel (eluent:hexane/ethyl acetate=10/1) gave ethyl 2-[4-(2-bromoacetyl)-3-chlorophenoxy]-2-methylpropionate (204 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696489B1
Source datasetuspto-grants-2004_02
ORD IDord-6298bc1b1fe247a6bac1a5a48b720a64
Source noteuspto-grants-2004_02