HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(2-chloroethyl)-6-methoxy-2(1H)-quinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(2-hydroxyethyl)-6-methoxy-2(1H)-quinolone | HCID 21846025 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(2-chloroethyl)-6-methoxy-2(1H)-quinolone | HCID 15388699 | 94.8% |
Reaction Steps
3.4 ml (46.6 mmol) of thionyl chloride are added while stirring at room temperature to a suspension of 3.11 g (14.2 mmol) of 4-(2-hydroxyethyl)-6-methoxy-2(1H)-quinolone in 50 ml of chloroform and 3 drops of dimethylformamide. The suspension is heated to reflux for 14 hours (total solubilization). After cooling to room temperature, 50 ml of water are added dropwise to the reaction medium and the mixture is left stirring for 30 minutes. The organic phase is recovered, separated after settling has taken place, washed with water, dried over magnesium sulphate and filtered. The filtrate is concentrated under vacuum. 3.2 g of a pale yellow solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958924 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-599b4728d02a4e8e9058a51457ac7392 |
| Source note | uspto-grants-1999_09 |