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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506149Generated: October 30, 2026

Trifluoroacetic acid → 4-(2-Aminoethyl)benzonitrile

https://huagongshe.com/reaction/1506149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-cyanophenethylcarbamateHCID 21955533—
SolventDichloromethaneHCID 6344—
Product4-(2-Aminoethyl)benzonitrileHCID 2191252540%

Reaction Steps

tert-Butyl 4-cyanophenethylcarbamate (305 mg, 1.24 mmol) in dichloromethane (4 mL) was mixed with trifluoroacetic acid (3.50 mL, 47.1 mmol) under cooling with ice and then stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, mixed with saturated aqueous potassium carbonate and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound as a pale orange solid (72.5 mg, yield 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-9999292718f04924bdd8c1cdc9c80ea9
Source noteuspto-grants-2015_12