HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047591Generated: October 30, 2026
6-(Trifluoromethyl)pyridine-3-carboxaldehyde → (NE)-2-methyl-N-[[6-(trifluoromethyl)-3-pyridinyl]methylidene]propane-2-sulfinamide
https://huagongshe.com/reaction/1047591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-(Trifluoromethyl)pyridine-3-carboxaldehyde | HCID 2777762 | — |
| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | (NE)-2-methyl-N-[[6-(trifluoromethyl)-3-pyridinyl]methylidene]propane-2-sulfinamide | HCID 87094737 | 107.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569512B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-ffb912e814464ba49802ab8d2beaca60 |
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| Source note | uspto-grants-2013_10 |
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