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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396777Generated: October 29, 2026

Methyl iodide → 2-Phenylmethyl-4-isopropyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide

https://huagongshe.com/reaction/2396777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Phenylmethyl-4-isopropyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 54267297—
SolventTetrahydrofuranHCID 8028—
Product2-Phenylmethyl-4-isopropyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxideHCID 1942444388%

Reaction Steps

To a solution of potassium t-butoxide (3.53 g, 29 mmol) in THF was added to a solution of 2-phenylmethyl-4-isopropyl-1, 2,5-thiadiazolidin-3-one 1,1-dioxide (7.7 g, 29 retool) in THF at 0° C. and the mixture was stirred at this temperature for 1 hour. To the mixture was added methyl iodide (20.38 g, 0.143 mol) and the resulting mixture was allowed to stir at room temperature for 2.5 hours. The resulting mixture was quenched with brine, extracted with ether, and the organic layer was washed with brine. The organic layer was dried, concentrated in vacuo, and the residue was purified by flash chromatography to afford 7.1 g (88%) of 2-phenylmethyl-4-isopropyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula XI: R1 =H; R2 =isopropyl; R3 =CH3) as a solid, m.p. 52.5°-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05494925
Source datasetuspto-grants-1996_02
ORD IDord-f630f4aadd7b4746ad0e7d59975128cd
Source noteuspto-grants-1996_02