HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 3-(10,11-Dihydro-5h-dibenz[b,f]azepin-5-ylmethyl)-1-piperidylacetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylcarbonyl)-1-benzylpiperidine hydrogen oxalate hemihydrate | HCID 131722490 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(10,11-Dihydro-5h-dibenz[b,f]azepin-5-ylmethyl)-1-piperidylacetic acid ethyl ester | HCID 53834894 | 87% |
Reaction Steps
A mixture of the above piperidine (2.05 g, 7 mmol), ethyl bromoacetate (1.36 g, 8.1 mmol), potassium carbonate (1.7 g, 12.3 mmol) and acetone (50 ml) was heated at reflux temperature under stirring for 7 h. The mixture was filtered and the solvent evaporated in vacuo. The oily residue was purified on silica gel (20 g) using ethyl acetate as eluent to give 2.3 g (87%) 3-(10,11-dihydro-5H-dibenz[b,f]azepin-5-ylmethyl)-1-piperidylacetic acid ethyl ester as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214816B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-5205845a8cd64092b676e2771e162424 |
| Source note | uspto-grants-2001_04 |