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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828189Generated: November 2, 2026

Methanesulfonyl chloride → HCID 17952495, compound

https://huagongshe.com/reaction/1828189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 17952496HCID 17952496—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
SolventSodium BicarbonateHCID 516892—
ProductHCID 17952495HCID 1795249580%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Cyclobutyl-5-hydroxymethyl-3-methyl-1,3-dihydro-benzoimidazol-2-one (13.79 g, 59.4 mmol) was diluted with dichloromethane (300 mL) and triethylamine (12.4 mL). The reaction was cooled to 0° C. and methanesulfonyl chloride (6.9 mL, 89.1 mmol) was added. The mixture was stirred for 1 hour at 0° C. then was diluted with saturated sodium bicarbonate and extraced into dichloromethane. The organic layer was dried over sodium sulfate and concentrated. The resulting oil was filtered through silica gel using ethyl acetate containing 1% triethylamine as eluent to give 11.92 g of 5-Chloromethyl-1-cyclobutyl-3-methyl-1,3-dihydro-benzoimidazol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056918B2
Source datasetuspto-grants-2006_06
ORD IDord-8ef8c35e96754e58bdd8326a36d816f5
Source noteuspto-grants-2006_06