HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-Bromo-1-(1-naphthalenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 1-Acetylnaphthalene | HCID 13663 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-1-(1-naphthalenyl)ethanone | HCID 3830513 | — |
Reaction Steps
Methyl 1-naphthyl ketone (10.1 g.), in 50 ml of a 1:1 mixture of chloroform and ethyl acetate is treated with 26.5 g. of copper (II) bromide. The resulting reaction mixture is heated under reflux with vigorous stirring until the evolution of hydrogen bromide ceases. When the reaction is complete the solvent is removed, ether is added and the copper (I) bromide is removed by filtration. Evaporation of the filtrate under reduced pressure yields crude bromomethyl 1-naphthyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04150153 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-1489e7152d2f4faab50106df544efc62 |
| Source note | uspto-grants-1979_04 |