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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061560Generated: November 1, 2026

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

https://huagongshe.com/reaction/2061560

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 3, 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 numberUS08283365B2
Source datasetuspto-grants-2012_10
ORD IDord-c113bb0d2a694fce8eaf522046dd9a5c
Source noteuspto-grants-2012_10