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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192281Generated: November 2, 2026

Triethylamine → HCID 58408289, compound

https://huagongshe.com/reaction/2192281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
Reactant5-BromoindolineHCID 3411566—
SolventDichloromethaneHCID 6344—
ProductHCID 58408289HCID 58408289—

Reaction Steps

5.09 g of commercially available 4-cyano-benzenesulfonyl chloride were dissolved in 125 ml dichloromethane. Then 5.0 g 5-Bromo-2,3-dihydro-1H-indole were added followed by 12.2 ml triethylamine. The mixture was stirred at room temperature for thirty minutes. Then the solvent was removed in vacuo. The residue was diluted with 100 ml of ethyl acetate and the mixture washed with 100 ml water and 100 ml saturated NaHCO3 solution. The organic layer was then dried over MgSO4. The solvent was removed in vacuo. The resulting crude material was purified by chromatography on silica gel to obtain 5.46 g of 4-(5-Bromo-2,3-dihydro-indole-1-sulfonyl)-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329725B2
Source datasetuspto-grants-2012_12
ORD IDord-e8a8bd2f91944294807dce24bdfed64d
Source noteuspto-grants-2012_12