HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 6-Bromo-1,2,3,4-tetrahydronaphthalen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Bromo-1-tetralone | HCID 10105069 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 18469932 | 94% |
Reaction Steps
To a solution of 6-bromo-1,2,3,4-tetrahydronaphthalen-1-one (2.0 g, 8.9 mmol) in EtOH (20 mL) was added NaBH4 (1.6 g, 42.7 mmol) at rt, and the reaction was stirred for 30 min. The reaction was diluted with water (10 mL) and extracted with EtOAc (3×50 mL). Organics were washed with brine (50 mL), dried (Na2SO4) and concentrated to give 1.9 g (94%) of the title compound as a brown oil. [M+H] calc'd for C10H11BrO2, 227, 229. found 227, 229.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447046B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d8692e0a624043d49fcbd98aacc92b89 |
| Source note | uspto-grants-2016_09 |