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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328198Generated: October 30, 2026

Acetic Acid → 2-(1,1,2,2-Tetrachloroethylsulfenylmercapto)-4-methyl pyridine

https://huagongshe.com/reaction/328198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrachloroethylsulfenyl chlorideHCID 20211738—
Reactant2-Mercapto-4-methylpyrimidine hydrochlorideHCID 178428687—
Product2-(1,1,2,2-Tetrachloroethylsulfenylmercapto)-4-methyl pyridineHCID 54039898—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension was prepared by mixing 3.4 g (0.02 mol) 2-mercapto-4-methyl pyrimidine hydrochloride in 100 ml of acetic acid. Then 5.0 g (0.02 mol) of tetrachloroethylsulfenylchloride was added to this suspension all at once. The resulting mixture was stirred at the reflux temperature for 3 minutes. At the end of this time the reaction mixture was filtered while hot. The filtrate was evaporated to 10 ml by volume. This material was then diluted with 100 ml of benzene and 75 ml of hexane and cooled to 0° C. The precipitate was removed by filtration and discarded. The filtrate was evaporated to give a liquid which crystallized upon standing. The crystals were separated by filtration and after drying weighed 3.3 g. The product, 2-(1,1,2,2-tetrachloroethylsulfenylmercapto)-4-methyl pyrimidine, had a melting point of 54°-56° C. Analysis was as follows: %Cl, calc. 43.8, found 43.2; %S, calc. 19.8, found 18.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016275
Source datasetuspto-grants-1977_04
ORD IDord-bcc7a27164964d1390a40d18d04bcbb2
Source noteuspto-grants-1977_04