HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Benzaldehyde 4-(4-chloro-alpha-cyanobenzyl)-3,5-dichlorophenyl hydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 4-(4-Chloro-alpha-cyanobenzyl)-3,5-dichlorophenyl hydrazine | HCID 22008537 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzaldehyde 4-(4-chloro-alpha-cyanobenzyl)-3,5-dichlorophenyl hydrazone | HCID 86754869 | — |
Reaction Steps
In 30 ml of acetic acid ethyl ester was dissolved 3.26 g of 4-(4-chloro-α-cyanobenzyl)-3,5-dichlorophenyl hydrazine. To the solution was added equimolar benzaldehyde and three times as much mol. of anhydrous magnesium sulfate, then the reaction was allowed to proceed for one hour at room temperature. After completion of the reaction, insolubles were removed, and the solution was concentrated, which was recrystallized from acetonitrile to afford 3.3 g of the titled compound as colorless crystals, m.p.162-163° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211178B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-1498695bf0a84033b1a6147d20c71936 |
| Source note | uspto-grants-2001_04 |