HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-Methoxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 7-Methoxy-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene | HCID 12415146 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Methoxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one | HCID 12415147 | 93% |
Reaction Steps
A solution of 7-methoxy-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene (Intermediate 8, 1.65 g, 8.7 mmol) in 7.5 mL of glacial acetic acid was cooled to 0° C. and treated with a solution of chromium trioxide (2 g, 20 mmol) in 8mL of acetic acid and 7 mL of water. The reaction mixture was then allowed to warm to ambient temperature and stirred overnight. It was diluted with water and extracted with diethyl ether (×2). The combined organic phase was washed with water (×1), saturated aqueous sodium bicarbonate (×1) and brine (×1), dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title compound (1.64 g, 93%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855512B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-372f3c86a1f54b10a1e19e5c78854c00 |
| Source note | uspto-grants-2005_02 |