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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396776Generated: October 29, 2026

Sulfuryl chloride → 2-Chloromethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide

https://huagongshe.com/reaction/2396776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2-Phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 19424449—
SolventDichloromethaneHCID 6344—
Product2-Chloromethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 15837478—

Reaction Steps

To a solution of 2-phenylthiomethyl-4-propyl-5-methyl-l,2,5-thiadiazolidin-3-one 1,1-dioxide (8.4 g) in 150 ml of methylene chloride was added sulfuryl chloride (3.22 ml) and the mixture was stirred for 3 hours at room temperature. The mixture was concentrated in vacuo and the residue triturated in hexane (150 ml) for 2 hours. The solvent was concentrated in vacuo and the residue was purified by flash chromatography (silica gel) to afford 5.7 g of 2-chloromethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1dioxide (Formula II: R1 =H; R2 =propyl; R3 =CH3 ; X'=Cl) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494925
Source datasetuspto-grants-1996_02
ORD IDord-8864682b21da49d7a52190acf9365c56
Source noteuspto-grants-1996_02