HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthalen-1-ylpropan-1-one → 2-Bromo-1'-propionaphthone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthalen-1-ylpropan-1-one | HCID 231159 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1'-propionaphthone | HCID 231161 | 175.6% |
Reaction Steps
To a solution of 1-(naphth-1-yl)-1-propanone (4.0 g) in anhydrous tetrahydrofuran (50 ml) was added phenyltrimethylammonium tribromide (8.0 g). The resulting mixture was stirred overnight at room temperature then partitioned between petroleum ether and aqueous sodium carbonate solution. The organic layer was separated, washed with water, brine, dried with sodium sulphate, filtered and evaporated in vacuo to yield crude 2-bromo-1-(naphth-1-yl)-1-propanone (5.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429607B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-6f9b7a4872db46e69235876df70a9231 |
| Source note | uspto-grants-2008_09 |