Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909100Generated: November 1, 2026

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

https://huagongshe.com/reaction/1909100

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 numberUS08598209B2
Source datasetuspto-grants-2013_12
ORD IDord-fbd34e5a4e8a4a01bdd50bcb1f051805
Source noteuspto-grants-2013_12