HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-oxopiperidine-1-carboxylate → 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | 2-Bromo-4-isopropyl-cyclohexanone | HCID 62708067 | — |
| Product | 1-tert-Butyloxycarbonyl-3-bromo-4-oxopiperidine | HCID 10683970 | — |
Reaction Steps
The bromination of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester takes place in a manner similar to that described above for the preparation of 2-bromo-4-isopropyl-cyclohexanone. The title compound is reacted as a crude product without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07727979B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-0f91e36356c443afb325cec8d55ab4f8 |
| Source note | uspto-grants-2010_06 |