HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 13394076, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | HCID 178469623 | HCID 178469623 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 13394076 | HCID 13394076 | — |
Reaction Steps
4.6 Grams of ethyl 7-acetamido-4-hydroxy-3-quinolinecarboxylate are dissolved in 15 ml of 10% NaOH, 60 ml of H2O and 100 ml of ethanol, and 5 ml of ethyl bromide are added. The mixture is left under reflux for 4 hours, then the excess of ethyl bromide and ethanol is evaporated off, and 10 ml of 10% NaOH are then added. The mixture is heated under reflux for 2 hours, allowed to cool, acidified with HCl, filtered and treated with ethanol at 70° C. The product is filtered off and recrystallized in a dimethylformamide/water (1:1) mixture. 1.0 Gram of a solid is obtained, of melting point 304°-307° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04552882 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-c954ab24e3934f1eb1e31ee71cb60546 |
| Source note | uspto-grants-1985_11 |