HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4,4-Dimethyl-1,2,3,4-tetrahydronaphthalen-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4,4-Dimethyl-3,4-dihydro-2H-naphthalen-1-one | HCID 236547 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene methanol | HCID 21867641 | — |
| Product | 4,4-Dimethyl-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 12643032 | — |
Reaction Steps
To a stirred suspension of sodium borohydride (3.5 g, 93 mmoles) in dry methanol (50 ml) at 0° C. under a nitrogen atmosphere was added a solution of 4,4-dimethyl-1-tetralone (10 g, 57.4 mmoles) in dry methanol:toluene (1:3) dropwise over a 45 minute period. After this time the mixture was allowed to warm to room temperature, and then two volumes of water were added. After stirring for 1 hour, the organic layer was separated, dried over magnesium sulfate, filtered, and evaporated under reduced pressure to leave a light yellow oil. This was purified by silica gel column chromatrography eluting with ethyl acetate:hexane (1:9) to give 1,2,3,4-tetrahydro-4,4-dimethyl-1-naphthol as a colorless oil. (9.89 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663337 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-980985d05c05472dbbceb82e193c84b0 |
| Source note | uspto-grants-1997_09 |