HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1(2H)-Naphthalenone, 3,4-dihydro-6-(2-propenyloxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 136337044 | HCID 136337044 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1(2H)-Naphthalenone, 3,4-dihydro-6-(2-propenyloxy)- | HCID 11701234 | — |
Reaction Steps
3.30 ml of allyl bromide was added to a mixture consisting of 5.62 g of 6-hydroxy-3,4-dihydroxynaphthalen-1(2H)-one, 5.27 g of potassium carbonate, and 60 ml of acetone. The obtained mixture was heated to reflux under nitrogen atmosphere overnight. The reaction solution was cooled to a room temperature, and the precipitate was removed by filtration. The solvent was removed under a reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain 6.35 g of the subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538123B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-ecfd8e5583e44cf2b952aecc7d991ee2 |
| Source note | uspto-grants-2009_05 |