HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dichloroethane → 7-(Benzyloxy)-5-(chloroacetyl)quinolin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Acetyl-7-(benzyloxy)quinolin-2(1H)-one | HCID 21072849 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Trimethylbenzylammonium Dichloroiodate | HCID 56924451 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-(Benzyloxy)-5-(chloroacetyl)quinolin-2(1H)-one | HCID 21072859 | — |
Reaction Steps
7.0 g (23.9 mmol) 5-acetyl-7-benzyloxy-1H-quinolin-2-one and 19.0 g (54.6 mmol) benzyltrimethylammonium dichloriodate are stirred in 43 mL acetic acid, 7 mL water and 147 mL dichloroethane at 65° C. After 4.5 hours the reaction is stopped by the addition of 400 mL sodium carbonate solution and 50 mL 5% sodium bisulphite solution. The insoluble constituents are suction filtered, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307076B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-1316f7ce2acc4134bbde8c29190d53cd |
| Source note | uspto-grants-2007_12 |