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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239559Generated: October 31, 2026

Trifluoroacetic acid → 4-(2-Aminoethyl)benzonitrile

https://huagongshe.com/reaction/2239559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-cyanophenethylcarbamateHCID 21955533—
SolventDichloromethaneHCID 6344—
Product4-(2-Aminoethyl)benzonitrileHCID 2191252574.3%

Reaction Steps

tert-Butyl [2-(4-cyanophenyl)ethyl]carbamate (1.14 g, 4.62 mmol) was dissolved in DCM (6 mL) and TFA (5 mL) was added. The mixture was concentrated and dissolved in EtOAc, and the organic phase was washed with saturated aqueous K2CO3. The organic layer was dried with Na2SO4, filtered and evaporated affording the title compound (0.50 g, 74.3%). 1H NMR (500 MHz, CDCl3): δ 1.21 (bs, 2H), 2.81 (t, 2H), 2.99 (t, 2H), 7.31 (d, 2H), 7.58 (d, 2H); 13C NMR (125 MHz, CDCl3): δ 40.38, 43.31, 110.33, 119.23, 129.86, 132.48, 145.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723333B2
Source datasetuspto-grants-2010_05
ORD IDord-e482b70022d04d83be2e3b5f09f9f809
Source noteuspto-grants-2010_05