HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 7,8-Dihydro-2-(phenylmethoxy)-5(6H)-quinolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 2-Hydroxy-7,8-dihydro-5(6H)-quinolinone | HCID 267450 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7,8-Dihydro-2-(phenylmethoxy)-5(6H)-quinolinone | HCID 10444977 | 92% |
Reaction Steps
A mixture of 7,8-dihydro-1H,6H-quinoline-2,5-dione (20.4 g, 125.0 mmoL), benzyl bromide (17.8 mL, 150 mmoL) and 20.8 g, 75 mmoL) in toluene (250 mL) was stirred at room temperature for 3 days under the protection from light. The reaction was stopped, filtered through celite and rinsed with a mixture of methylene chloride and methanol. The filtrate was concentrated and trituated in petroleum ether (150 mL). Filtration of the mixture provided the desired product (29.4 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605265B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-04894738ec954b35b3d7e61e2b6cf196 |
| Source note | uspto-grants-2009_10 |