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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624272Generated: October 26, 2026

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

https://huagongshe.com/reaction/624272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTert-ButanesulfinamideHCID 3382465—
Reactant3-OxetanoneHCID 15024254—
CatalystHCID 178477244HCID 178477244—
SolventSodium chloride; waterHCID 57417360—
Product2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamideHCID 46839995—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a 250 mL round-bottomed flask was added 2-methylpropane-2-sulfinamide (3.36 g, 27.8 mmol) followed by tetraethoxytitanium (11.64 ml, 55.5 mmol) to a tetrahydrofuran (69.4 ml) solution of oxetan-3-one (2 g, 27.8 mmol) at room temperature. The mixture was stirred at 50° C. for 5 hours, cooled and poured into brine. The suspension was filtered through a pad of diatomaceous earth eluting with ethyl acetate. The organics were combined, dried with sodium sulfate, filtered and concentrated under vacuum. The residue was purified by regular phase flash column chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302989B2
Source datasetuspto-grants-2016_04
ORD IDord-3d453ee755554741a9d6bc4cb6c12527
Source noteuspto-grants-2016_04