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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576376Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 22908742, compound

https://huagongshe.com/reaction/1576376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodiumHCID 5360545—
ReactantHCID 178526649HCID 178526649—
SolventAcetonitrileHCID 6342—
ProductHCID 22908742HCID 22908742—

Reaction Steps

A solution of 3.5 g. of phenylsulfonyl chloride in 20 m. of anhydrous acetonitrile was added to a solution of 6.4 g. of 4-nitro-2,6-bis(trifluoromethyl)benzimidazole, sodium salt in 50 ml. of anhydrous acetonitrile. The mixture was stirred at room temperature for 2 hours, and the reaction mixture was filtered. The filtrate was evaporated to dryness under vacuum, and the residue was recrystallized from benzenepentane to yield 4-nitro-1-phenylsulfonyl-2,6-bis(trifluoromethyl)benzimidazole, m.p. 183°-185°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03980784
Source datasetuspto-grants-1976_09
ORD IDord-17fdf2478dec419c9fd7a25493114b26
Source noteuspto-grants-1976_09