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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743431Generated: October 30, 2026

Benzyl Bromide → 2-Phenylmethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide

https://huagongshe.com/reaction/743431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant4-Propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 18922248—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product2-Phenylmethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 1892225739.2%

Reaction Steps

To a mixture of 4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (5.0 g, 28.25 mmol) suspended in 150 ml of toluene was added phenylmethyl bromide (5.32 g, 31.03 mmol) and tetrabutylammonium bromide (0.9 g, 0.28 mmol). The resulting mixture was refluxed for 19 hours, cooled, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography to afford 2.97 g (39%) of 2-phenylmethyl-4-propyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula IX: R1 =H; R2 =propyl) as a solid, m.p., 63.5°-65.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556909
Source datasetuspto-grants-1996_09
ORD IDord-4c7f8976d9fd47fba04dd21f336b7899
Source noteuspto-grants-1996_09