HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Phenyl-1,2,2a,3,4,5-hexahydrobenz[cd]indol-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Benzoyl-2-phenyl-1,2,2a,3,4,5-hexahydrobenz[cd]indol-5-one | HCID 19348301 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Phenyl-1,2,2a,3,4,5-hexahydrobenz[cd]indol-5-one | HCID 19348287 | 111.1% |
Reaction Steps
A portion (4.25 g) of the compound obtained in Example 1 was dissolved in ethanol (40 ml). To the solution was added conc. hydrochloric acid (40 ml) and the resulting mixture was heated to reflux for 2 hours. After allowing to cool, the mixture was diluted with water, adjusted to pH 9 with potassium carbonate and extracted three times with ethyl acetate. The organic layers were combined, washed with saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure and the residue was crystallized from an ether/hexane mixed solvent to yield 3.33 g (92%) of the titled compound as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06040331 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-0fe79847ea854760944a0e9f26b3988d |
| Source note | uspto-grants-2000_03 |