HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709913Generated: October 29, 2026
Acetic Acid → 6-(Benzyloxy)-2-bromo-1,2,3,4-tetrahydronaphthalen-1-ol
https://huagongshe.com/reaction/709913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-(Benzyloxy)-2-bromo-3,4-dihydronaphthalen-1(2h)-one | HCID 23087083 | — |
| Product | 6-(Benzyloxy)-2-bromo-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 23087248 | 91.8% |
Reaction Steps
6-Benzyloxy-2-bromo-3,4-dihydro-2H-naphthalen-1-one (32.9 g, 0.0964 mol) was dissolved in ether (200 mL, 2 mol) and methanol (30.0 mL, 0.740 mol), cooled with ice bath to internal temperature of 3° C. Sodium tetrahydroborate (1.82 g, 0.0482 mol) was added portionwise over 15 min at 3° C.-8° C. (internal). The mixture was stirred at 2-5° C. for 1 hour. Acetic acid (2.74 mL, 0.0482 mol) was added and the mixture was quenched with water, extracted with EtOAc (100 mL), washed with water (2×), brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give a crude intermediate, 6-(benzyloxy)-2-bromo-1,2,3,4-tetrahydronaphthalen-1-ol (29.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181191B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-64f58c4619154d6b9a46c179ddc0ee1f |
|---|
| Source note | uspto-grants-2015_11 |
|---|