Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993745Generated: October 30, 2026

4-(Bromoacetyl)benzonitrile → 4-{2-[(2-Hydroxy-1,1-dimethylethyl)amino]-1,3-thiazol-4-yl}benzonitrile

https://huagongshe.com/reaction/1993745

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantN-(1-Hydroxy-2-methylpropan-2-yl)thioureaHCID 22768414—
SolventEthanolHCID 702—
Product4-{2-[(2-Hydroxy-1,1-dimethylethyl)amino]-1,3-thiazol-4-yl}benzonitrileHCID 86618598100%

Reaction Steps

This compound was prepared in the same manner as described in step 3 of Example 6. 4-(2-bromoacetyl)benzonitrile (1.7 g, 7.4 mmol) and N-(2-hydroxy-1,1-dimethylethyl)thiourea (1.1 g, 7.4 mmol), prepared in step 2 of Example 3, were heated to reflux in 45 mL of ethanol for 30 min. The reaction mixture was cooled to room temperature and the crude product was collected by suction filtration to give 4-{2-[(2-hydroxy-1,1-dimethylethyl)amino]-1,3-thiazol-4-yl}benzonitrile (2.0 g, 100%), MS (ES) m/z 274 [M+H]+. No further purification was performed on this compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652018B2
Source datasetuspto-grants-2010_01
ORD IDord-08fdf228e0854dab82b05a3d62b1891a
Source noteuspto-grants-2010_01