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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11236Generated: October 26, 2026

Benzenesulfonyl chloride → 1-Phenylsulfonylpyrrole

https://huagongshe.com/reaction/11236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantPyrroleHCID 8027—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-PhenylsulfonylpyrroleHCID 140146736.9%

Reaction Steps

To a suspension of sodium hydride (60% in mineral oil, 2.4 g, 60 mmol) in DMF (100 ml) was added dropwise at an ice bath temperature a solution of pyrrole (3.35 g, 50 mmol) in DMF (5 ml). The mixture was stirred for 30 minutes at room temperature and cooled again. To the mixture was added dropwise a soluton of benzenesulfonylchloride (9.7 g, 5.5 mmol) in DMF (3 ml). The mixture was stirred for 30 minutes at room temperature and poured into ice-water, and extracted with ethylacetate. The extract was washed with water and dried. The solvent was evaporated. The obtained crystal was washed with hexane to give 1-benzenesulfonylpyrrole (8.4 g). Yield: 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098201B2
Source datasetuspto-grants-2006_08
ORD IDord-a974fa5d025a477aaee1506f61791129
Source noteuspto-grants-2006_08