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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165643Generated: October 27, 2026

Benzenesulfonyl chloride → 1H-Indole, 3-acetyl-1-(phenylsulfonyl)-

https://huagongshe.com/reaction/2165643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant3-AcetylindoleHCID 12802—
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium ChlorideHCID 25517—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product1H-Indole, 3-acetyl-1-(phenylsulfonyl)-HCID 848535—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 41.39 g of 3-acetyl indole in 300 ml of dimethyl sulfoxide at 0° C. was added a solution of 18.6 g of potassium hydroxide in 20 ml of water. This mixture was stirred at 0° C. for 2 hours, then 47.6 ml of benzenesulfonyl chloride was added dropwise over 40 minutes. The mixture was stirred for an additional 30 minutes, then poured into aqueous ammonium chloride and extracted several times with ether. The ether extracts were combined, washed with water, dried and evaporated, giving 59.8 g of 3-acetyl-N-phenylsulfonyl indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04940710
Source datasetuspto-grants-1990_07
ORD IDord-2b93cceae6c045508a234743f73a4884
Source noteuspto-grants-1990_07