HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydro-1H-cyclopenta[a]naphthalen-1-one → HCID 10103867, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydro-1H-cyclopenta[a]naphthalen-1-one | HCID 240454 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10103867 | HCID 10103867 | — |
Reaction Steps
A 12.36 g portion of benzindanone (63 mmole) was dissolved in 300 ml of THF and 150 ml of methanol, and 3.6 g (95 mmole) of sodium borohydride was added at room temperature. After stirring the mixture for 6 hours, the reaction was terminated with dilute hydrochloric acid, and extracted with hexane (100 ml X 2) and ether (100 ml×2). Two stereoisomers of benzindanol were obtained. The crude product was used for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05942459 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-271fef6bd4ea4967ba88e29f3dc3b570 |
| Source note | uspto-grants-1999_08 |