HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 3,4-Dihydro-6-methoxy-2-methylene-1(2h)-naphthalenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| Reactant | N-Methylanilinium trifluoroacetate | HCID 2724109 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Dihydro-6-methoxy-2-methylene-1(2h)-naphthalenone | HCID 11344469 | — |
Reaction Steps
A mixture of 6-methoxytetralone (29.24 g, 165.9 mmol), paraformaldehyde (22.4 g, 746.6 mmol) and N-methylanilinium trifluoroactate (55 g, 248.9 mmol) in 250 mL THF was refluxed for 4 hours and allowed to come to room temperature. To this was added ether (250 mL) with stirring and the mixture was decanted to remove the gummy precipitate. The supernatant was washed with sat. NaHCO3, the oganic layer was dried (MgSO4) and concentrated. The residue was redissolved in ether, filtered through celite and concentrated to afford the title compound as a thick yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664250B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-c7eb14bfbdd84499bd6a79efe0b6eb5b |
| Source note | uspto-grants-2003_12 |