HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylnaphthalene → 2-Naphthoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylnaphthalene | HCID 7122 | — |
| Reactant | 2-Naphthoic acid | HCID 7123 | — |
| Reactant | Diboron | HCID 6328200 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 2-Naphthoic acid | HCID 7123 | — |
| Product | 2-Naphthalenemethanol | HCID 74128 | — |
Reaction Steps
2-Acetylnaphthalene is prepared by treating 2-(1-bromoethyl)naphthalene, prepared as described above, with sodium acetate in acetic acid to afford 2-(1-acetoxyethyl)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 | US04009197 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-fee330c163c5406791381ec023d45b83 |
| Source note | uspto-grants-1977_02 |