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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381716Generated: November 2, 2026

Phenacyl bromide → HCID 21276526, compound

https://huagongshe.com/reaction/1381716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 21276516HCID 21276516—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21276526HCID 21276526—

Reaction Steps

N-methyl-2-(4-methylaminocarbonylmethoxyphenyl)-1-methylethanamine hydrochloride (2.73 g) was suspended in tetrahydrofuran (10 ml) containing triethylamine (6 ml) and a solution of α-bromoacetophenone (1.99 g) in tetrahydrofuran (10 ml) was added dropwise. After stirring overnight this solution was treated with saturated sodium carbonate solution, extracted with dichloromethane, the organic phase was dried (magnesium sulphate), filtered and evaporated to give a red oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803293
Source datasetuspto-grants-1989_02
ORD IDord-d6086f0e5bab4a30ba3fd15725708941
Source noteuspto-grants-1989_02