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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420116Generated: October 27, 2026

Triethylamine → 5,6-Dichloro-1-(methylsulphonyl)-benzimidazole

https://huagongshe.com/reaction/2420116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5,6-Dichloro-1H-benzimidazoleHCID 331775—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product5,6-Dichloro-1-(methylsulphonyl)-benzimidazoleHCID 20313044—

Reaction Steps

A solution of methanesulphonyl chloride (60 parts) in acetone (800 parts) was added dropwise to a suspension of 5,6-dichloro-benzimidazole (94 parts) in acetone (240 parts) containing triethylamine (50 parts). A precipitate of triethylamine hydrochloride was observed and the temperature rose to 40° C. The mixture was heated under reflux for 10 minutes and then stirred at room temperature for 20 hours. On pouring into cold water (4000 parts) a solid product precipitated out, which was filtered off, washed with water, dried and recrystallised from acetone (charcoal) to give 5,6-dichloro-1-(methylsulphonyl)-benzimidazole (61 parts) as pale yellow needles, melting point 191°-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04109004
Source datasetuspto-grants-1978_08
ORD IDord-4a8e25bb60ef4025aae0c947bbe4344a
Source noteuspto-grants-1978_08