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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471617Generated: October 30, 2026

Trifluoroacetic acid → 2-Amino-6-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/471617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(4-Methoxybenzylamino)-6-(trifluoromethyl)benzonitrileHCID 67399920—
Product2-Amino-6-(trifluoromethyl)benzonitrileHCID 2262519599.9%

Reaction Steps

2-(4-Methoxybenzylamino)-6-(trifluoromethyl)benzonitrile (Example 144c) (3.49 g, 11.4 mmol) was treated with trifluoroacetic acid (TFA) (35 mL) at 0° C., and then stirred at room temperature for 20 min. The TFA was removed under vacuum, and the residue was dissolved in CH2Cl2 (150 mL) and washed with 1M NaOH. The organic layer was dried with MgSO4, filtered and removed under vacuum. The crude product was purified by chromatography on silica gel eluting with CH2Cl2 to give 2.12 g (99%) 2-amino-6-(trifluoromethyl)benzonitrile as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 7.45 (m, 1H), 7.07 (m, 1H), 6.96 (m, 1H), 6.60 (br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633186B2
Source datasetuspto-grants-2014_01
ORD IDord-99920a3029894967bca9c3eef208c57f
Source noteuspto-grants-2014_01