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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide | HCID 46839995 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507683B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-f2e18a1a779344948eb942a5e07e06fa |
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| Source note | uspto-grants-2013_08 |
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