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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401204Generated: November 1, 2026

2-(trifluoromethyl)-1H-indole-5-carbonitrile → (2-(Trifluoromethyl)-1h-indol-5-yl)methanamine

https://huagongshe.com/reaction/2401204

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(trifluoromethyl)-1H-indole-5-carbonitrileHCID 58126812—
SolventTetrahydrofuranHCID 8028—
Product(2-(Trifluoromethyl)-1h-indol-5-yl)methanamineHCID 58126817—

Reaction Steps

A solution of 2-trifluoromethyl-1H-indole-5-carbonitrile (Intermediate 33, 0.16 g, 0.761 mmol) in tetrahydrofuran (5 mL) cooled in an ice-water bath, was treated with a 1M solution of borane tetrahydrofuran complex (3.05 mL, 3.05 mmol) dropwise via syringe. The reaction mixture was then left to stir under argon for 18 hrs while allowing it to warm to room temperature. The reaction mixture was then quenched with methanol (10 mL) and stirred at room temperature for 10 min. The reaction mixture was then poured onto a SCX cartridge (10 g) and washed well with methanol. The desired product was then eluted using 2M ammonia/methanol solution. Evaporation to dryness gave the title compound which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796283B2
Source datasetuspto-grants-2014_08
ORD IDord-bf337eea572c4642aaa96983cc9880cf
Source noteuspto-grants-2014_08