HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 6-Bromo-2-naphthyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-Bromo-2-naphthalenol | HCID 27144 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Bromo-2-naphthyl acetate | HCID 80655 | — |
Reaction Steps
6-bromo-2-naphthol is obtained according to the procedure of Example 1. A solution of acetic anhydride, sodium acetate, and the 6-bromo-2-naphthol in toluene is then refluxed for about 2 1/2 hours. Crude 2-acetoxy-6-bromonaphthalene is isolated therefrom by stripping the solvent from the organic layer after washing with water. The acetoxy compound is then purified by recrystallization from n-butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04374262 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-e1a8512ff5344a95911414fff27ad5db |
| Source note | uspto-grants-1983_02 |