Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67981364 | HCID 67981364 | 93% |
Reaction Steps
4-Iodobenzaldehyde (1.26 g, 5.43 mmol) was dissolved in dichloromethane (41.8 mL). 2-methylpropane-2-sulfinamide (0.679 g, 5.43 mmol) was added, followed by titanium(IV) ethoxide (2.25 mL, 10.9 mmol). The reaction was heated to reflux for 1 hour. The reaction was then allowed to cool to room temperature and stir for 18 hours. Methanol (8.0 mL) and saturated sodium bicarbonate (1.5 mL) were added to the reaction mixture. The resulting slurry was filtered through sodium sulfate, and rinsed with ethyl acetate. The filtrate was concentrated to yield the title compound N-(4-iodobenzylidene)-2-methylpropane-2-sulfinamide (1.69 g, 93%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 8.51 (s, 1H), 7.80-7.84 (m, 2H), 7.53-7.57 (m, 2H), 1.25 (s, 9H). MS (M+1): 336.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056834B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-1bfd913a3b284a6bb078b15a73076c5d |
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| Source note | uspto-grants-2015_06 |
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