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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191076Generated: November 1, 2026

4-(Bromoacetyl)benzonitrile → HCID 59828836, compound

https://huagongshe.com/reaction/1191076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2,2,2-Trifluoroethyl)thioureaHCID 20202812—
SolventEthanolHCID 702—
ProductHCID 59828836HCID 5982883695.3%

Reaction Steps

Slurry 4-cyanophenacyl bromide (1.4 g, 6.3 mmol), 2,2,2-trifluoroethyl-thiourea (1.0 g, 6.3 mmol) and sodium bicarbonate (529 mg, 6.3 mmol) in absolute ethanol (30 mL). Stir the mixture at reflux for 1 h under a nitrogen atmosphere. Cool to room temperature and concentrate in vacuo. Partition the residue between DCM (100 mL) and water (20 mL). Dry the organic layer over Na2SO4 and concentrate in vacuo to obtain the desired intermediate (1.7 g, 95%). MS (ES+) m/z: 284 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680091B2
Source datasetuspto-grants-2014_03
ORD IDord-d4a371b13503439f922b45fee5d47658
Source noteuspto-grants-2014_03