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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Catalyst | HCID 178477244 | HCID 178477244 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide | HCID 46839995 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302989B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-3d453ee755554741a9d6bc4cb6c12527 |
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| Source note | uspto-grants-2016_04 |
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