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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396775Generated: October 29, 2026

Chloromethyl phenyl sulphide → 2-Phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide

https://huagongshe.com/reaction/2396775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl phenyl sulphideHCID 81623—
Reactant4-Propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 18922253—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product2-Phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 1942444988%

Reaction Steps

A mixture of 4-propyl-5-methyl-1, 2,5-thiadiazolidin-3-one 1,1-dioxide (9 g) , phenylthiomethyl chloride (7.43 g) and tetrabutylammonium bromide (1 g) was suspended in 200 ml of toluene, refluxed for 8 hours, cooled, and concentrated in vacuo. The residue was purified by flash chromatography (15-20% ethyl acetate in hexane) to afford 8.5 g (88%) of 2-phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula VI: R1 =H; R2 =propyl; R3 =CH3) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494925
Source datasetuspto-grants-1996_02
ORD IDord-7052a37f66f1443399e412d8aa6fe661
Source noteuspto-grants-1996_02