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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892549Generated: October 29, 2026

Tert-Butanesulfinamide → 2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide

https://huagongshe.com/reaction/1892549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButanesulfinamideHCID 3382465—
Reactant3-OxetanoneHCID 15024254—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamideHCID 46839995—

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Methylpropane-2-sulfinamide (3.36 g, 27.77 mmol, 1 eq) and Ti(OEt)4 (12 ml, 55.54 mmol, 2 eq) were added to a solution of oxetan-3-one (2 g, 27.77 mmol, 1 eq) in THF at 22° C. The reaction mixture was stirred at 50° C. for 5 h. It was cooled to room temperature and poured into saturated brine solution, and then the suspension was filtered through a pad of Cellite. The filtrate was extracted with ethyl acetate, and the organic layer washed with saturated brine solution, dried over Na2SO4 and concentrated. The crude product was purified by silica gel (60-120 mesh) columatography using 30% EtOAc/Petroleum ether. Yield: 0.55 g (45.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507683B2
Source datasetuspto-grants-2013_08
ORD IDord-f2e18a1a779344948eb942a5e07e06fa
Source noteuspto-grants-2013_08