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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056450Generated: November 1, 2026

Pyridine → HCID 131736427, compound

https://huagongshe.com/reaction/1056450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,3,3-Tetrafluoro-1-propanolHCID 6441—
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantPyridinium chlorideHCID 10176127—
ProductHCID 131736427HCID 131736427—

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 HCF2CF2CH2OH (445.35 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, ethanesulfonyl chloride (411.4 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-f9c9fd3e89fb4865a9e15ffb39ce9fb3
Source noteuspto-grants-2016_07