HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dihydroxybenzaldehyde → HCID 136607406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Reactant | HCID 940183 | HCID 940183 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136607406 | HCID 136607406 | 66% |
Reaction Steps
In ethanol (30 ml), 5-(2,4-dichlorophenyl)-2H-pyrazole-3-carboxylic acid hydrazide (136 mg) prepared in the Step 21-1-1 and 2,4-dihydroxybenzaldehyde (69 mg) was heated under reflux for 29 hours. Crystal appeared as the mixture was concentrated under a reduced pressure, the resulting crystal was separated by filtration, washed with ethanol, washed with ethyl acetate, and dried to give the title compound (129 mg, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200008B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-1b8fd1b819da4a0a9d749ba0c2e7599b |
| Source note | uspto-grants-2015_12 |