HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509308Generated: October 25, 2026
tert-Butylsulfinamide, (S)-(-)- → (NE,S)-2-methyl-N-[[3-(trifluoromethyl)pyridin-2-yl]methylidene]propane-2-sulfinamide
https://huagongshe.com/reaction/509308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butylsulfinamide, (S)-(-)- | HCID 11355477 | — |
| Reactant | 3-(Trifluoromethyl)pyridine-2-carboxaldehyde | HCID 14761470 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (NE,S)-2-methyl-N-[[3-(trifluoromethyl)pyridin-2-yl]methylidene]propane-2-sulfinamide | HCID 89310312 | — |
Reaction Steps
To a solution of 3-(trifluoromethyl)picolinaldehyde (Frontier Scientific, 9.80 g, 56.0 mmol) and DCM (50 mL) was added (S)-2-methylpropane-2-sulfinamide (AK Scientific, 10.3 g, 85.0 mmol) and copper(II) sulfate (35.3 g, 221 mmol). After 1.5 h at rt, the reaction was filtered through a pad of Celite® brand filter agent and rinsed with DCM. The filtrate was concentrated in vacuo to give a dark green oil. The oil thus obtained was loaded onto a silica gel column and eluted with 30% EtOAc in hexanes to give (S,E)-2-methyl-N-((3-(trifluoro-methyl)pyridin-2-yl)methylene)propane-2-sulfinamide, as a golden oil. 1H NMR (δ ppm, CDCl3, 300 MHz): 9.02 (d, J=4.3 Hz, 1H), 8.70 (d, J=1.3 Hz, 1H), 8.38 (d, J=7.7 Hz, 1H), 7.79 (dd, J=7.9 & 4.8 Hz, 1H), 1.18 (s, 9H). MS (ESI pos. ion) m/z: 279.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096527B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-08d4c08fa9d5440794b1021424f0ac7e |
|---|
| Source note | uspto-grants-2015_08 |
|---|