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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716663Generated: October 27, 2026

Chlorosulfonyl isocyanate → 4-Bromo-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/1716663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant4-BromoindoleHCID 676494—
SolventAcetonitrileHCID 6342—
Product4-Bromo-1H-indole-3-carbonitrileHCID 2763232—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 4-bromoindole (5 g, 25.5 mmol) in acetonitrile (50 ml) was added dropwise chlorsulfonylisocyanate (2.37 ml, 27.3 mmol) over a 5 minute period. The reaction mixture was stirred at 0° C. for 2 hours, and TEA (3.77 ml, 27.0) was added dropwise over a 10 minute period. The reaction mixture was allowed reach room temperature overnight, poured into ice/water mixture (200 ml), and the aqueous layer was extracted with EtOAc. The combined organic extracts were dried over Na2SO4, filtered, concentrated, and purified by flash chromatography to afford 4-bromo-1H-indole-3-carbonitrile LVII as an off-white solid (4.9 g, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-f71d0473fa5b42a8b07b70b4a9f07b2d
Source noteuspto-grants-2010_09