HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → 4-(4-Bromophenyl)-4-fluoro-1-methylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | 4-(4-bromophenyl)-1-methyl-3,6-dihydro-2H-pyridine | HCID 10634535 | — |
| Reactant | 4-(4-Bromophenyl)-1-methylpiperidin-4-ol | HCID 10659634 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Bromophenyl)-4-fluoro-1-methylpiperidine | HCID 58266526 | — |
Reaction Steps
To a solution of DAST (0.50 g, 3.8 mmol) in CH2Cl2 was added a solution of 4-(4-bromophenyl)-1-methylpiperidin-4-ol (0.507 g, 1.88 mmol) in CH2Cl2 at −78° C. The resulting mixture was warmed to rt over a period of 3 h. The reaction was then allowed to cool to 0° C. and quenched with saturated NaHCO3. The resulting mixture was extracted with CH2Cl2 and the combined organic extracts were dried over MgSO4 and concentrated to give a yellow oil. The crude product was purified by silica gel chromatography (95:5 EtOAc/NH3 to 10:8:2 CH2Cl2/MeOH/NH3) to yield an inseparable mixture of the title compound and 4-(4-bromophenyl)-1-methyl-1,2,3,6-tetrahydropyridine (280 mg, used without further purification).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481533B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-17e338c6fa76401785325169d3939b77 |
| Source note | uspto-grants-2013_07 |