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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040064Generated: October 31, 2026

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

https://huagongshe.com/reaction/1040064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButanesulfinamideHCID 3382465—
Reactant3-OxetanoneHCID 15024254—
CatalystTitanium tetraethoxideHCID 76524—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamideHCID 4683999538.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of oxetan-3-one (600 mg, 8.33 mmol) and 2-methylpropane-2-sulfinamide (1.01 g, 8.33 mmol) in tetrahydrofuran (14 mL), titanium ethoxide (3.45 mL, 16.65 mmol) was added. The mixture was stirred at 50° C. overnight. The reaction mixture was poured over brine. The suspension was filtered through celite and washed with ethyl acetate. The solution was partitioned between ethyl acetate and brine. The organics were dried (Na2SO4), filtered and concentrated. The residue was purified by column chromatography on silica (0-70% ethyl acetate in hexanes) to afford 2-methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide (692 g, 3.20 mmol, 38% yield) as a clear oil. MS ESI: [M+H]+ m/z 176.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551984B2
Source datasetuspto-grants-2013_10
ORD IDord-f5194beed50c42bbaf492f22817f26c8
Source noteuspto-grants-2013_10