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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660153Generated: October 29, 2026

Phenacyl bromide → HCID 20558013, compound

https://huagongshe.com/reaction/1660153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant(2-Phenylethyl)thioureaHCID 735845—
SolventEthanolHCID 702—
ProductHCID 20558013HCID 2055801381%

Reaction Steps

N-phenethylthiourea (225 grams, 1.25 moles) and α-bromoacetophenone (250 grams, 1.25 moles, Aldrich Chem. Co.) in 1500 ml absolute ethanol were heated to reflux temperature for 21/2 hours under nitrogen. After reducing the solvent volume by 10%, the reaction mixture was cooled to room temperature and then to 0° C. in an ice bath. The solids were filtered off, redissolved in 2,500 ml of absolute ethanol and heated to reflux. The solvent volume was reduced to 2000 ml and the reaction mixture cooled to 0° C. This procedure was repeated and after the second recrystallization the solids were collected and dried under vacuum over phosphorous pentoxide, yielding 365 grams (81%) of 2-phenethylamino-4-phenyl-thiazole hydrobromide, m.p. 169°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307106
Source datasetuspto-grants-1981_12
ORD IDord-97691aaa5b5b48bda268ee6ef7825ddc
Source noteuspto-grants-1981_12