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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745277Generated: November 1, 2026

Methanesulfonyl chloride → HCID 13655348, compound

https://huagongshe.com/reaction/745277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 13655347HCID 13655347—
SolventPyridineHCID 1049—
ProductHCID 13655348HCID 13655348—

Reaction Steps

To a stirred and cooled (ice-bath) mixture of 22 parts of 2,4-dichloro-β-(cyclohexylmethyl)benzeneethanol and 50 parts of pyridine are added dropwise 8.8 parts of methanesulfonyl chloride. Upon completion, stirring is continued for 3 hours at room temperature. The reaction mixture is poured onto water and the product is extracted twice with trichloromethane. The combined extracts are washed twice with a diluted hydrochloric acid solution and once with water, dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane, yielding 16.5 parts of 3-cyclohexyl-2-(2,4-dichlorophenyl)propyl methanesulfonate; mp. 105.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04598085
Source datasetuspto-grants-1986_07
ORD IDord-b57e9eeabebb423aac11900eb6ad1fef
Source noteuspto-grants-1986_07