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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743420Generated: October 25, 2026

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

https://huagongshe.com/reaction/743420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl phenyl sulphideHCID 81623—
Reactant4-Propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 18922248—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product2-Phenylthiomethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 1942446563%

Reaction Steps

To a mixture of 4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (5.1 g, 28.65 mmol)suspended in 210 ml of toluene was added phenylthiomethyl chloride (4.93 g, 31.49 mmol) and tetrabutylammonium bromide (0.92 g, 2.86 mmol). The resulting mixture was refluxed for 18 hours, cooled, filtered, and the filtrate was concentrated in vacuo. The residue was purified by column chromatography to afford 5.39 g (63%) of 2-phenylthiomethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula VI: R1 =H; R2 =propyl; R3 =H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556909
Source datasetuspto-grants-1996_09
ORD IDord-091ec06c42eb402eafb47269a8e00dc0
Source noteuspto-grants-1996_09