HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-hydroxy-N'-(1-phenylmethylene)-2-naphthohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 3-Hydroxy-2-naphthoic acid hydrazide | HCID 72699 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-hydroxy-N'-(1-phenylmethylene)-2-naphthohydrazide | HCID 689876 | — |
Reaction Steps
A four neck flask (2 liters) equipped with a thermometer, a reflux condenser and a stirrer was charged with 101 g (0.5 mol) of 3-hydroxy-2-naphthohydrazide and 1.5 liter of methanol, and 63.7 g (0.6 mol) of benzaldehyde was dropwise added thereto in 30 minutes while stirring at room temperature. After heating under reflux for 5 hours, the reaction liquid was cooled down to 15° C. or lower, and crystal was filtered off. The crystal was washed with a small amount of methanol and then dried under reduced pressure, whereby the intended compound (slightly yellow crystal) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06380288B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-10e9640f5ca84d77865d4cf45ce33d7c |
| Source note | uspto-grants-2002_04 |