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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061666Generated: November 3, 2026

Phenacyl bromide → HCID 22284323, compound

https://huagongshe.com/reaction/1061666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantTriethylamineHCID 8471—
Reactant2-MercaptoacetamideHCID 12961—
SolventEthanolHCID 702—
ProductHCID 22284323HCID 22284323—

Reaction Steps

Triethylamine (4.55 g) is added to a solution of 2-mercaptoacetamide (8.00 g, Reference compound No. 40-1) in ethanol (70 ml), then phenacyl bromide (17.5 g) is added to the mixture, and the whole is stirred for four hours. The reaction mixture is concentrated under reduced pressure, water and 0.1 N hydrochloric acid are added to the resulting residue, and the whole is extracted with ethyl acetate. The extract is washed with saturated brine and dried over anhydrous magnesium sulfate. The extract is concentrated under reduced pressure. The resulting residue is suspended in ethanol (200 ml), p-toluenesulfonic acid monohydrate (catalytic amount) is added to the suspension, and the mixture is refluxed for five days. The reaction mixture is cooled to room temperature to precipitate crystals. The crystals are filtered off and washed with ethanol to give the titled reference compound (11.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960575B2
Source datasetuspto-grants-2005_11
ORD IDord-9b6d8e40e6d7468693c38672ecfd7465
Source noteuspto-grants-2005_11