HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one → 5-(2-chloroacetyl)-8-phenylmethoxy-1H-quinolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one | HCID 13375444 | — |
| Reactant | Trimethylbenzylammonium Dichloroiodate | HCID 56924451 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 5-(2-chloroacetyl)-8-phenylmethoxy-1H-quinolin-2-one | HCID 10903550 | — |
Reaction Steps
25.2 g (86 mmol) 5-acetyl-8-benzyloxy-1H-quinolin-2-one (European Journal of Medicianl Chemistry 1984, 19(4), 341) and 50 g (142 mmol) benzyltrimethylammonium dichloriodate in 500 mL dichloroethane and 300 mL methanol are stirred overnight at reflux temperature. The reaction mixture is evaporated down and the residue is stirred overnight in THF and 1 N hydrochloric acid. After the THF has been distilled off the precipitated solid is suction filtered, washed with diethyl ether and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307076B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-a11f8d532aa14756850f9b24b7421726 |
| Source note | uspto-grants-2007_12 |