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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTert-ButanesulfinamideHCID 3382465—
ReactantSodium borohydrideHCID 4311764—
Reactant3,4-Bis(difluoromethoxy)benzaldehydeHCID 14509269—
CatalystTitanium tetraethoxideHCID 76524—
SolventTetrahydrofuranHCID 8028—
ProductN-[3,4-bis(difluoromethoxy)benzyl]-2-methylpropane-2-sulfinamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399494B2
Source datasetuspto-grants-2013_03
ORD IDord-6340a433b9bf4bf0b9aca4834c4e7b25
Source noteuspto-grants-2013_03