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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592265Generated: October 30, 2026

6-(Trifluoromethyl)pyridine-3-carboxaldehyde → (NE)-2-methyl-N-[[6-(trifluoromethyl)-3-pyridinyl]methylidene]propane-2-sulfinamide

https://huagongshe.com/reaction/592265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Trifluoromethyl)pyridine-3-carboxaldehydeHCID 2777762—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
CatalystCopper SulfateHCID 24462—
Solvent1,1-DichloroethaneHCID 6365—
Product(NE)-2-methyl-N-[[6-(trifluoromethyl)-3-pyridinyl]methylidene]propane-2-sulfinamideHCID 87094737107.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 6-(trifluoromethyl)nicotinaldehyde (45.0 g, 257 mmol) in dichloroethane (640 mL) were added (S)-(−)-2-methyl-2-propanesulfinamide (34.3 g, 283 mmol) and anhydrous copper(II) sulfate (82 g, 514 mmol). The mixture was stirred at 50° C. After 48 h, the mixture cooled to ambient temperature. The reaction mixture was filtered through Celite. The filtered cake was washed with dichloromethane and the filtrate was concentrated to give the title compound (76.8 g). MS 223.1 (M-tert-butyl+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238647B2
Source datasetuspto-grants-2016_01
ORD IDord-d66d2d7feacf4f56ba2112c25cc5b2b2
Source noteuspto-grants-2016_01