HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 5-Acetyl-7-(benzyloxy)quinolin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 5-acetyl-7-benzyloxy-3,4-dihydro-1H-quinolin-2-one | HCID 21072850 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Acetyl-7-(benzyloxy)quinolin-2(1H)-one | HCID 21072849 | — |
Reaction Steps
13.0 g (44 mmol) 5-acetyl-7-benzyloxy-3,4-dihydro-1H-quinolin-2-one are suspended in 130 mL dioxane and combined with 15.0 g (66 mmol) 2,3-dichloro-5,6-dicyanobenzoquinone. The mixture is refluxed for 30 minutes, cooled to ambient temperature and stirred for a further 2 hours. The solid is filtered off, washed with dioxane and dissolved in 600 mL dichloromethane/methanol (9:1). The solution is washed with sodium hydrogen carbonate solution, dried with sodium sulphate and evaporated down. Then the residue is suspended in methanol, filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307076B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-132ffd4a82154e4fb6c268bce98fffc0 |
| Source note | uspto-grants-2007_12 |