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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370757Generated: October 26, 2026

tert-Butylsulfinamide, (R)-(+)- → (R)-2-methyl-N-((4-(trifluoromethyl)pyridin-3-yl)methylene)propane-2-sulfinamide

https://huagongshe.com/reaction/2370757

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
Reactant4-(Trifluoromethyl)pyridine-3-carbaldehydeHCID 21354724—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
Product(R)-2-methyl-N-((4-(trifluoromethyl)pyridin-3-yl)methylene)propane-2-sulfinamideHCID 71144309—

Reaction Steps

To a the solution of 4-(trifluoromethyl)nicotinaldehyde from above was added DCM (10 mL), (R)-2-methylpropane-2-sulfinamide (1.553 g, 12.81 mmol; See Table 1, footnote 1) (AK Scientific) and copper sulfate (4.09 g, 25.6 mmol) (Aldrich, anhydrous). The suspension was stirred at rt under N2 for 68 h. The suspension was then filtered through Celite® brand filter agent, and the solid was washed with DCM (2×20 mL). The filtrates were concentrated and purified by ISCO (40 g, SiO2, 10-50% EtOAc/hexane) to give (R)-2-methyl-N-((4-(trifluoromethyl)pyridin-3-yl)methylene)propane-2-sulfinamide as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710043B2
Source datasetuspto-grants-2014_04
ORD IDord-6aae6a7c016d40b9b4f9058691ba60f6
Source noteuspto-grants-2014_04