HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → Tert-butyl 3-fluoro-4-oxopiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Selectfluor | HCID 2724933 | — |
| Reactant | tert-Butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate | HCID 10778540 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 3-fluoro-4-oxopiperidine-1-carboxylate | HCID 10560711 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of tert-butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate (5.00 g, 18.40 mmol) in dry acetonitrile (25 mL) was added Selectfluor® (7.55 g, 20.3 mmol) at rt. The reaction mixture was stirred at rt for 2 h then poured into EA and successively washed with aq. 1% NaHCO3 and brine. The org. layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by FC (hexanes/EA, 4:1) to afford the title compound as a pale yellow solid. LC-MS-conditions 08: tR=0.55 min; [M-CH3+H]+=203.23; TLC: rf (hexanes/EA, 4:1)=0.17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09139524B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-fb3ce4ad9c124b35b754e6b0acbe4916 |
| Source note | uspto-grants-2015_09 |