Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantTriethylamineHCID 8471—
ReactantPyBroPHCID 2733179—
ReactantPyridine, 4-(difluoromethyl)-, 1-oxideHCID 90015270—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
ProductN-tert-butyl-4-(difluoromethyl)pyridin-2-amineHCID 9001529965%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399636B2
Source datasetuspto-grants-2016_07
ORD IDord-a2a0f222d2ad4652b9f30c5e94e21303
Source noteuspto-grants-2016_07