HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 2-Acetylnaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-(1-Bromoethyl)naphthalene | HCID 18678254 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Acetylnaphthalene | HCID 7122 | — |
Reaction Steps
2-Acetylnaphthalene is prepared by treating 2-(1'-bromoethyl)naphthalene, prepared as described above, wtih sodium acetate in acetic acid to afford 2-(1'-acetonyethyl)naphthalene which upon base hydrolysis furnishes the 2-(1'-hydroxyethyl)naphthalene. The latter is oxidized with an equivalent of chromium trioxide in glacial acetic acid, or 8N sulfuric acid and acetone to furnish 2-acetylnaphthalene. 2-Carboxynaphthalene is prepared from 2-acetylnaphthalene by treating the latter with aqueous sodium hypochlorite. The 2-carboxynaphthalene is treated with diborane in an ether, such as diglyme (diethyleneglycol dimethyl ether), to yield 2-hydroxymethylnaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04048330 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-b1bb5bfd9aa8461d8402d868f2dd79b1 |
| Source note | uspto-grants-1977_09 |