HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | tert-Butyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate | HCID 10778540 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine | HCID 10683970 | 87.8% |
Reaction Steps
NBS (1.4 g) was added to a solution of 1-tert-butoxycarbonyl-1,2,3,6-tetrahydro-4-(trimethylsilyloxy)pyridine (2 g) in acetonitrile and the mixture was stirred at room temperature for 30 minutes. The solution was diluted with ethyl acetate(50 ml) and washed with water (50 ml), sodium bicarbonate solution (50 ml) and brine (50 ml), dried (MgSO4) and evaporated to give the title compound as a colourless solid (1.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506773B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-9e50011067924b0aa3bd679630e21393 |
| Source note | uspto-grants-2003_01 |