HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22413568, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22413579 | HCID 22413579 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22413568 | HCID 22413568 | 97.7% |
Reaction Steps
A mixture of 3,4-dihydro-6-(2-quinolylmethoxy)-1(2H)-naphthalenone (1.82 g, 6 mmol), prepared as in step 2, and sodium borohydride (230 mg, 6 mmol) in ethanol (15 mL) was refluxed for 30 minutes. The reaction was allowed to warm to ambient temperature and was then quenched with saturated NH4Cl. Extraction with ethyl acetate and purification on a silica gel column eluting with 9:1 CH2Cl2 -ethyl acetate afforded 1.79 g of 1,2,3,4-tetrahydro-6-(2-quinolylmethoxy)-1-naphthalenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05512581 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-46e7568f9f5948ca864b76f6017de91d |
| Source note | uspto-grants-1996_04 |