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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413293Generated: October 23, 2026

Methanol → N-[2-(4-Bromoacetyl-phenyl)-ethyl]-acetamide

https://huagongshe.com/en/reaction/413293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantn-[2-(4-Acetylphenyl)ethyl]acetamideHCID 237789—
ReactantTetra-n-butylammonium tribromideHCID 23500184—
SolventDichloromethaneHCID 6344—
ProductN-[2-(4-Bromoacetyl-phenyl)-ethyl]-acetamideHCID 1852361783%

Reaction Steps

In a round-bottomed flask, N-[2-(4-acetyl-phenyl)-ethyl]-acetamide (7.23 g, 35.2 mmol) was dissolved in methylene chloride (120 ml), and methanol (60 ml). Tetrabutylammonium tribromide (17.0 g, 35.2 mmol) was added to this solution in one portion, and the mixture was allowed to stir overnight at room temperature. The volatiles were then removed in vacuo to afford an oil, which was then resuspended in 100 ml of methylene chloride and extracted with 125 ml of saturated aqueous sodium bicarbonate. The aqueous extracts were reextracted with methylene chloride (3×100 ml), and the combined organic extracts were then washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude oil was purified by column chromatography (silica gel; methylene chloride to 7% methanol/methylene chloride), and the resulting material was washed with 110 ml of water to afford 8.27 g (83% yield) of pure product as a white solid. LRMS ([M−1 ]−)=283.0, 284.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566377B2
Source datasetuspto-grants-2003_05
ORD IDord-5b0af00a054b4c3cbc0168762c8e172e
Source noteuspto-grants-2003_05