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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475178Generated: October 30, 2026

4-Toluenesulfonyl chloride → 1-tosyl-1H-indole-6-carbonitrile

https://huagongshe.com/reaction/475178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium hydrideHCID 24758—
Reactant1H-indole-6-carbonitrileHCID 85146—
SolventTetrahydrofuranHCID 8028—
Product1-tosyl-1H-indole-6-carbonitrileHCID 7127195367.5%

Reaction Steps

To a solution of 1H-indole-6-carbonitrile (70 mg, 0.5 mmol, CASRN 15861-36-6) in THF (5 mL) cooled to 0° C. was added with vigorous stirring NaH (25 mg, 60% in oil, 0.65 mmol). After stirring for 30 min, TsCl (140 mg, 0.75 mmol) was added to the mixture. The reaction mixture was stirred at RT for 18 h then partitioned between DCM (300 mL) and water (50 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated in vacuo. The resulting residue was purified by SiO2 chromatography eluting with a petroleum ether/EtOAc gradient (5 to 10% EtOAc) to afford 100 mg (67%) of 1-tosyl-1H-indole-6-carbonitrile (34) as a white solid: MS (ESI) m/z=297.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637537B2
Source datasetuspto-grants-2014_01
ORD IDord-8d3ca324e10943979ed0eb2765541c17
Source noteuspto-grants-2014_01