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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725344Generated: October 31, 2026

Methanesulfonyl chloride → HCID 86605221, compound

https://huagongshe.com/reaction/1725344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 22036323HCID 22036323—
SolventPyridineHCID 1049—
ProductHCID 86605221HCID 8660522151%

Reaction Steps

A solution of 2-(3,5-difluoro-phenoxy)-ethanol (2.5 g, 14.3 mmol) in pyridine (10 ml) was cooled with an ice bath and treated dropwise with methanesulfonyl chloride (1.7 g, 14.7 mmol). The ice bath was removed and the mixture was stirred for 16 hours at room temperature. The pyridine was evaporated in vacuo and the residue was dissolved in ethyl acetate. The organic phase was washed with water, with 2N hydrochloric acid then three times with water, dried over magnesium sulfate and concentrated. The residue was crystallised in diisopropyl ether to give methanesulfonic acid 2-(3,5-difluoro-phenoxy)-ethyl ester (1.8 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491714B2
Source datasetuspto-grants-2009_02
ORD IDord-697f9ca91d7543d088ef17e3d0826572
Source noteuspto-grants-2009_02