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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709276Generated: October 30, 2026

2-(Dimethylamino)ethyl acrylate → 2-(Acryloyloxy)-N-[(4-benzoylphenyl)methyl]-N,N-dimethylethan-1-aminium bromide

https://huagongshe.com/reaction/1709276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethyl acrylateHCID 17111—
Reactant4-(Bromomethyl)benzophenoneHCID 122951—
SolventAcetoneHCID 180—
Product2-(Acryloyloxy)-N-[(4-benzoylphenyl)methyl]-N,N-dimethylethan-1-aminium bromideHCID 2206259749.04%

Reaction Steps

Dimethylaminoethyl acrylate (9.11 mls) was added to a stirred solution of 4-bromomethylbenzophenone (13.75g) in acetone (50 mls) at 55° C. and the mixture was stirred for two hours at 60°±2° C. After cooling to room temperature, the stirred mixture was further cooled in an ice bath for two hours prior to filtration. After washing the residue with acetone (X1) followed by isopropyl ether (X2) the solid was dried under vacuo at room temperature. The crude title compound was obtained as a white crystalline solid (14.48g; m.p. 121°-123° C.) which was recrystallised from acetone (150 mls). Filtration, followed by sequentially washing with acetone (X1) then isopropyl ether (X1) and drying under vacuo at room temperature gave the title compound (10.26g; yield =49.04%) as white fine granular crystals of melting point equal to 122°-124° C. Analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948819
Source datasetuspto-grants-1990_08
ORD IDord-e14e25336fe24562ac81546389c1937c
Source noteuspto-grants-1990_08