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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191069Generated: October 28, 2026

4-(Bromoacetyl)benzonitrile → 4-(2-Amino-1,3-thiazol-4-yl)benzonitrile

https://huagongshe.com/reaction/1191069

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantSodium BicarbonateHCID 516892—
ReactantThioureaHCID 2723790—
SolventEthanolHCID 702—
Product4-(2-Amino-1,3-thiazol-4-yl)benzonitrileHCID 2049589—

Reaction Steps

Slurry 4-cyanophenacyl bromide (40 g, 179 mmol), thiourea (13.6 g, 181 mmol) and sodium bicarbonate (15.3 g, 181 mmol) in absolute ethanol (560 mL). Stir the mixture at reflux for 20 h under a nitrogen atmosphere. Cool the slurry to room temperature, filter, wash the solids with ethanol (100 mL), water (3×75 mL) and hexane (3×75 mL). Collect the yellow solid, add water (200 mL) and stir the slurry for 30 min at room temperate. Filter and wash the solid with hexane (excess). Slurry the solid in EtOAc (50 mL) and concentrate in vacuo twice to remove residual water. Collect the desired intermediate as a light yellow solid (36 g, 99%). MS (ES+) m/z: 202.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680091B2
Source datasetuspto-grants-2014_03
ORD IDord-06f2fc3fe8a7410d849a4c8fe73f0ea8
Source noteuspto-grants-2014_03