HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948574Generated: October 31, 2026
Methanol → N-[3,4-bis(difluoromethoxy)benzyl]-2-methylpropane-2-sulfinamide
https://huagongshe.com/reaction/1948574
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Tert-Butanesulfinamide | HCID 3382465 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,4-Bis(difluoromethoxy)benzaldehyde | HCID 14509269 | — |
| Catalyst | Titanium tetraethoxide | HCID 76524 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3,4-bis(difluoromethoxy)benzyl]-2-methylpropane-2-sulfinamide | HCID 57484711 | — |
Reaction Steps
To a solution of 3,4-bis(difluoromethoxy)benzaldehyde (6-2, 100 mg, 0.42 mmol, 1 equiv) in THF (840 uL) was added 2-methylpropane-2-sulfinamide (56 mg, 0.46 mmol, 1.1 equiv) and titanium ethoxide (440 uL, 2.10 mmol, 5.0 equiv), and the reaction mixture stirred at ambient temperature for 4.5 hours. The reaction mixture was then cooled to 0° C. and sodium borohydride (31.8 mg, 0.84 mmol, 2.0 equiv) was added portionwise and the reaction was stirred for an additional hour. Methanol (2 mL) was added slowly and the reaction mixture was partitioned between EtOAc (20 mL) and brine (20 mL) and filtered. The organic phase was dried over MgSO4 and concentrated to afford crude N-[3,4-bis(difluoromethoxy)benzyl]-2-methylpropane-2-sulfinamide, which was dissolved in methanol (2.2 mL). To the solution was added HCl (2 M in ether, 655 uL, 3 equiv), and the reaction mixture stirred for 30 minutes. It was then concentrated to afford the desired product (6-3) as a white solid. ESI+MS [M-NH2]+ C9H7F4O2: 223.0 found, 223.0 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399494B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-6340a433b9bf4bf0b9aca4834c4e7b25 |
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| Source note | uspto-grants-2013_03 |
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