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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374671Generated: October 30, 2026

Phenacyl bromide → HCID 178512605, compound

https://huagongshe.com/reaction/2374671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 178513045HCID 178513045—
SolventAcetoneHCID 180—
ProductHCID 178512605HCID 17851260587%

Reaction Steps

A mixture of amidinothiourea (2.0 g, 16.9 mmol), 2-bromoacetophenone (3.4 g, 16.9 mmol) was heated at reflux in acetone (12 mL) for 4 h. The mixture was cooled to room temperature and removed half of the solvent. The precipitate was filtered, washed with acetone, and dried to give N-(4-phenyl-1,3-thiazol-2-yl)guanidine (3.2 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462723B2
Source datasetuspto-grants-2008_12
ORD IDord-2afeb05612be4a9e91a9768f0cc0264d
Source noteuspto-grants-2008_12