HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthol → 2-Acetyl-6-methoxynaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | 1-Bromo-2-methoxynaphthalene | HCID 72860 | — |
| Reactant | 1-(5-Bromo-6-methoxynaphthalen-2-yl)ethan-1-one | HCID 622178 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 2-Acetyl-6-methoxynaphthalene | HCID 77506 | — |
Reaction Steps
42 Ml of β-naphthol and 16.2 g of anhydrous aluminum chloride are added to the solution of 2-acetyl-5-bromo-6-methoxynaphthalene obtained as in example 1a), while keeping the temperature at -10° C. The reaction mixture is kept for 48 hours under stirring at room temperature and then it is worked as in example 1 with the only difference that the product is crystallized by isopropyl alcohol. 19 Grams of product are obtained with a yield equal to 38.7% calculated on the basis of the starting material 1-bromo-2-methoxynaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05107013 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-9148b56c102046959c02720002e6bd13 |
| Source note | uspto-grants-1992_04 |