HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 5-(Benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Hydroxy-1-tetralone | HCID 119921 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(Benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10586915 | 87.6% |
Reaction Steps
To a solution of 4.86 g of 5-hydroxy-1-tetralone in 50 ml of acetonitrile, 5.13 g of benzyl bromide and 6.22 g of potassium carbonate were added and the mixture was heated at reflux for 4 hours. The insoluble matter was removed by filtration and the filtrate was concentrated. The residue was purified by silica gel column chromatography to obtain 6.62 g of the desired compound as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205302B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-b8d41c52c76e4f0aa2b999fa80ced6aa |
| Source note | uspto-grants-2007_04 |