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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878398Generated: November 2, 2026

Methanesulfonyl chloride → HCID 86635134, compound

https://huagongshe.com/reaction/1878398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 66878475HCID 66878475—
SolventDichloromethaneHCID 6344—
ProductHCID 86635134HCID 86635134—

Reaction Steps

A solution of methanesulfonyl chloride (165 mg, 1.44 mmol) in dichloromethane (2.0 mL) was added to a stirred solution of N-tert-butyl-3-(1-hydroxy-2-methylpropyl)benzamide (300 mg, 1.20 mmol) in dichloromethane (8.0 mL). After 1.5 hours stirring, the mixture was partitioned between dichloromethane and aqueous sodium hydrogen carbonate solution. The aqueous layer was extracted with dichloromethane and the combined organic layers were washed with brine, dried over sodium sulfate and concentrated under vacuum to afford the intermediate 1-(3-(tert-butylcarbamoyl)phenyl)propyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314091B2
Source datasetuspto-grants-2012_11
ORD IDord-785ce14ec30445a49d59ec3fac58db43
Source noteuspto-grants-2012_11