Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230952Generated: October 30, 2026

Phenacyl bromide → N~1~-(4-Phenyl-1,3-thiazol-2-yl)benzene-1,3-diamine

https://huagongshe.com/reaction/2230952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantAcetamide, N-(3-((aminothioxomethyl)amino)phenyl)-HCID 6451295—
SolventEthanolHCID 702—
ProductN~1~-(4-Phenyl-1,3-thiazol-2-yl)benzene-1,3-diamineHCID 2272439482%

Reaction Steps

A mixture of N-(3-acetylaminophenyl)thiourea (0.84 g) and 2-bromoacetophenone (0.84 g) in ethanol (10 ml) was refluxed for 15 minutes. After evaporation of the solvent, 3N hydrochloric acid was added thereto and the mixture was refluxed for 30 minutes. The mixture was made basic with sodium bicarbonate and extracted with ethyl acetate. The organic solution was washed with water and brine, dried over magnesium sulfate and concentrated. The residue was crystallized from ethanol to give 3-(4-phenylthiazol-2-yl)aminoaniline (0.88 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426345B1
Source datasetuspto-grants-2002_07
ORD IDord-3e62d6a822974fd381d6f4cdfc42af94
Source noteuspto-grants-2002_07