HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 54162463, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | trans-1,2,3,4,4a,5,6,10b-Octahydro-benzo[f]quinoline | HCID 11030553 | — |
| Reactant | 4-(4-Phenylbenzoylamino)butyraldehyde | HCID 21712565 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 54162463 | HCID 54162463 | 46% |
Reaction Steps
Sodium triacetoxyborohydride (340 mg, 1.6 mmol) was added to a stirred mixture of trans-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinoline (D8a, 200 mg, 1 mmol), 4-(4-phenylbenzoylamino)butyraldehyde (286 mg, 01.1 mmol) and acetic acid (1 drop) in 1,2-dichloroethane (10 ml) at room temperature. After stirring for 16 h, dichloromethane (20 ml) was added and the mixture was then washed with saturated aqueous K2CO3 (2×25 ml) and brine (25 ml). Drying (Na2SO4) and evaporation in vacuo afforded an oil which was purified by preparative TLC on Kieselgel using 10% methanol-ethyl acetate as eluent to give the title compound as a colourless solid (200 mg, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080752 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-8b11a750a55e4a8ea382687e9ded0e60 |
| Source note | uspto-grants-2000_06 |