HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 54053829, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Chlorobenzohydrazide | HCID 10816 | — |
| Reactant | 4-Quinolinecarboxaldehyde | HCID 78072 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54053829 | HCID 54053829 | 85.1% |
Reaction Steps
A mixture of 7.86 gm (0.05 mole) of 4-quinolinecarboxaldehyde, 8.53 gm (0.05 mole) of 4-chlorobenzhydrazide, 400 ml of ethanol and 100 ml of tetrahydrofuran is refluxed 2 hr. Thin layer chromatography of the reaction mixture establishes that the reaction is complete. The reaction mixture is concentrated to one-half the original volume and then cooled to room temperature. The solid which separates is collected, washed with ethanol and dried to give 13.18 gm (85%) of title compound, having a melting point of 232.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04870082 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-5d035f0e81f843aab875ade41c08c5e9 |
| Source note | uspto-grants-1989_09 |