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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061567Generated: October 31, 2026

Water → 1-methyl-2-trifluoromethyl-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/2061567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-(trifluoromethyl)-1H-indole-5-carbonitrileHCID 58126812—
SolventDimethylformamideHCID 6228—
Product1-methyl-2-trifluoromethyl-1H-indole-5-carbonitrileHCID 58126825135.9%

Reaction Steps

Sodium hydride (60% in mineral oil) (76 mg, 1.903 mmol) was added to 2-trifluoromethyl-1H-indole-5-carbonitrile (Intermediate 3, 200 mg, 0.952 mmol) stirred in DMF (5 mL) under argon at room temperature. The reaction mixture was stirred at room temperature for 30 min and iodomethane (0.119 mL, 1.903 mmol) was then added. The reaction mixture was left to stir for a further 1 h. The reaction mixture was poured into water (50 mL) and extracted with ethyl acetate (50 mL). The organic extract was washed with 1:1 water: Brine (50 mL×2), dried (MgSO4), filtered and the solvent removed to give the title compound (290 mg) which was then used in the next reaction without further purification; 1H NMR (400 MHz, CDCl3): δ 8.05 (1H, d), 7.59 (1H, dd), 7.46 (1H, d), 7.03 (1H, s), 3.90 (3H, s); m/z 225 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283365B2
Source datasetuspto-grants-2012_10
ORD IDord-48d554eaed1f4870b54872ba18cd6529
Source noteuspto-grants-2012_10