HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054465Generated: October 31, 2026
tert-Butylsulfinamide, (S)-(-)- → HCID 178455581, compound
https://huagongshe.com/reaction/1054465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Reactant | HCID 118590572 | HCID 118590572 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178455581 | HCID 178455581 | 296.7% |
Reaction Steps
Titanium (IV) ethoxide (17.5 g, 76.92 mmol) was added to a solution of (S)-4-chloro-1-(5-fluoro-2-((tetrahydrofuran-3-yl)oxy)phenyl)butan-1-one (11 g, 38.46 mmol) and (S)-2-methylpropane-2-sulfinamide (9.32 g, 76.92 mmol) in THF (170 mL) with stirring. The mixture was stirred continuously at 70° C. for 16 h. Reaction mixture was then cooled to a temperature of 20-35° C., quenched with saturated aqueous NH4Cl solution, diluted with ethyl acetate and filtered. The filtrate was washed with water followed by brine solution. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 44.5 g of the title compound as a colorless liquid. MS (ESI): 390.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394305B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-625a1b284ccc4a54ac1a336c2a788784 |
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| Source note | uspto-grants-2016_07 |
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