HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-oxocyclohexanecarboxylate → Ethyl 3-bromo-4-oxocyclohexane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-oxocyclohexanecarboxylate | HCID 317638 | — |
| Reactant | 2-Bromo-4-isopropyl-cyclohexanone | HCID 62708067 | — |
| Product | Ethyl 3-bromo-4-oxocyclohexane-1-carboxylate | HCID 12917737 | — |
Reaction Steps
The bromination of 4-oxo-cyclohexane carboxylic acid ethyl 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-aa5614f3adf74aaeaa8e0d65a3012e4f |
| Source note | uspto-grants-2010_06 |