HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetylnaphthalene → 2-Bromo-1-(1-naphthalenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetylnaphthalene | HCID 13663 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Bromo-1-(1-naphthalenyl)ethanone | HCID 3830513 | 93.2% |
Reaction Steps
To a solution of 1-(naphthalen-1-yl)ethanone (500 mg, 2.9 mmol) in dioxane (5 mL) was added to a solution of bromine (510 mg, 3.19 mmol) in dioxane (10 mL), at room temperature, over a period of 30 minutes. The reaction mixture was then stirred at room temperature for 20 minutes and concentrated. The resulting residue was diluted with ether and washed with saturated sodium bicarbonate, water, dried over sodium sulfate and concentrated. Purification by preparative thin layer chromatography (70% DCM/30% hexanes) afforded 2-bromo-1-(naphthalen-1-yl)ethanone (673 mg, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372807B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-28433479610f4dd89803e5dd0db30856 |
| Source note | uspto-grants-2013_02 |