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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056451Generated: October 31, 2026

Pyridine → 2,2,2-Trifluoroethyl Methanesulfonate

https://huagongshe.com/reaction/1056451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantPyridinium chlorideHCID 10176127—
Product2,2,2-Trifluoroethyl MethanesulfonateHCID 556565—

Reaction Steps

A 10-L four-neck flask was equipped with a refluxing pipe and a dropping funnel to serve as a reactor. To the flask were added CF3CH2OH (337.1 g; 3.37 mol) and pyridine (306.31 g; 3.88 mol) in an ice bath, and the mixture was stirred. Using the dropping funnel, methanesulfonyl chloride (364.15 g; 3.20 mol) was dropped, with care for heat generation. The reaction solution changed its color gradually to milky white as pyridine hydrochloride was produced. After the end of the reaction, the reaction solution was washed with a 1 N HCl aqueous solution. The washed solution was separated to collect an organic layer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09397368B2
Source datasetuspto-grants-2016_07
ORD IDord-e0449065cd0742debd4aa4ce01398ae7
Source noteuspto-grants-2016_07