HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 12909379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 13152853 | HCID 13152853 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 12909379 | HCID 12909379 | — |
Reaction Steps
A suspension of 25 g. (0.070 mole) of 2,3-dibromo-6,11-dihydro-5 H-pyrrolo[2,1-b][3]benzazepin-11-one in 200 ml. ethanol containing 25 ml. of triethylamine and 1 gm. of 10% Pd on charcoal was hydrogenated under 3 atmospheres of hydrogen to yield 6,11-dihydro-5H-pyrrolo-[2,1-b][3]benzazepin-11-one, m.p. 54°-55° C. after removal of catalyst, recrystallization from petroleum ether and drying under vacuum. The same compound is also obtained by hydrogenolysis of the 2,3-dichloro ketone and the 1,2,3-tribromoketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075225 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-851ee8d9ae394760a9c3801f0269f95c |
| Source note | uspto-grants-1978_02 |