Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423751Generated: October 25, 2026

Chlorosulfonyl isocyanate → 6-Nitro-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/423751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant6-Nitro-1H-indoleHCID 78502—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product6-Nitro-1H-indole-3-carbonitrileHCID 28317982%

Reaction Steps

To a solution of 6-nitroindole (4.86 g 30 mmol) in DMF (24.3 mL) and CH3CN (243 mL) was added dropwise a solution of ClSO2NCO (5 mL, 57 mmol) in CH3CN (39 mL) at 0° C. After addition, the reaction was allowed to warm to room temperature and stirred for 2 h. The mixture was poured into ice-water, basified with sat. NaHCO3 solution to pH 7-8 and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated to give 6-nitro-1H-indole-3-carbonitrile (4.6 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101767B2
Source datasetuspto-grants-2012_01
ORD IDord-ba21c22babda4eadb1a280acb1e84a3c
Source noteuspto-grants-2012_01