HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dihydro-6,7-dimethoxy-1(2H)-naphthalenone → 6,7-Dimethoxy-1,2,3,4-tetrahydronaphthalen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dihydro-6,7-dimethoxy-1(2H)-naphthalenone | HCID 266816 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6,7-Dimethoxy-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 62735455 | 93% |
Reaction Steps
To a stirred solution of 6,7-dimethoxy-3,4-dihydronaphthalen-1(2H)-one (3.09 g, mmol) in MeOH (50 mL) was added NaBH4 (680 mg, 18 mmol) portion wise over 0.5 hour. The resulting mixture was stirred at room temperature overnight. The reaction was quenched with 1N HCl, diluted with water and extracted with DCM. The combined organic phase was washed with brine, dried over sodium sulfate and the solvent was removed under reduced pressure to afford 6,7-dimethoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a yellow oil (2.9 g, 93%). LC-MS (ES-API); rt 7.96 min; m/z calculated for C12H16O3 [M+Na]+ 231.1, found 231.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062076B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-329be3ed71694273b60b9bf989828d65 |
| Source note | uspto-grants-2015_06 |