HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → Diethyl 5-oxoazepane-1,4-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| Reactant | Ethyl diazodicarboxylate | HCID 86610729 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diethyl 5-oxoazepane-1,4-dicarboxylate | HCID 12485293 | — |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
To a cold solution (−30° C.) of 1-carbethoxypiperidin-4-one (3.0 ml, 26.5 mmol) in anhydrous ether, were simultaneously added a solution of boron trifluoride etherate (3.4 ml, 26.5 mmol) in diethyl ether (2.8 ml) and a solution of ethyl diazodicarboxylate (3.6 ml, 34.5 mmol) in diethyl ether (2.8 ml) over 1.5 hours via a syringe-pump. Upon completion of additions, the reaction mixture was allowed to stir for an additional hour at −30° C. and then warmed to room temperature. The reaction mixture was washed with 30% potassium carbonate and the organic phase was dried over Na2SO4 and concentrated in vacuo to give diethyl 5-oxoazepane-1,4-dicarboxylate as a crude yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07749994B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-7b69eb52042141b5b90c6e0f25005880 |
| Source note | uspto-grants-2010_07 |