HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057035Generated: November 2, 2026
Tert-Butylamine → N-tert-butyl-4-(difluoromethyl)pyridin-2-amine
https://huagongshe.com/reaction/1057035
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | Pyridine, 4-(difluoromethyl)-, 1-oxide | HCID 90015270 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-butyl-4-(difluoromethyl)pyridin-2-amine | HCID 90015299 | 65% |
Reaction Steps
A suspension of 4-difluoromethyl-pyridine-N-oxide (4.95 g, 34.1 mmol), bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (20.7 g, 44.3 mmol), triethylamine (15.6 mL, 111 mmol), and anhydrous tert-butylamine (4.6 mL, 43 mmol) in DCE (100 mL, 0.33 M) was sealed in pressure tube and stirred at 100° C. for 3.5 hr. After cooling to rt, the mixture was diluted with CH2Cl2 and washed with sat. aq. NaHCO3. The organics were dried over MgSO4 and following concentration, the reaction residue was purified by flash column chromatography (100:0-80:20 heptanes/EtOAc) to afford N-tert-butyl-4-(difluoromethyl)pyridin-2-amine as a yellow liquid (4.43 g, 65%); 1H NMR (400 MHz, CDCl3) δ 8.15 (d, J=5.2 Hz, 1H), 6.65-6.28 (m, 3H), 4.62 (br s, 1H), 1.44 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09399636B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a2a0f222d2ad4652b9f30c5e94e21303 |
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| Source note | uspto-grants-2016_07 |
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