HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Cyclohexanone 2,4-dinitrophenylhydrazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | (2,4-Dinitrophenyl)hydrazine | HCID 3772977 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Cyclohexanone 2,4-dinitrophenylhydrazone | HCID 74117 | 95% |
Reaction Steps
Concentrated sulfuric acid (2 mL) and 0.4456 g of 2,4-dinitrophenylhydrazine (2,4-DNP) were combined in a 25-mL Erlenmeyer flask. Water was added (2 to 3 mL) dropwise with swirling until the 2,4-DNP dissolved. This was followed by 10 mL of 95% ethanol. This solution was added, dropwise with swirling, to a solution of cyclohexanone, 0.5725 g, dissolved in 20 mL of 95% ethanol. A precipitate formed within 5 minutes. The mixture was refrigerated overnight. The precipitate was filtered to yield a yellow-orange crystalline solid. The product was re-crystallized from approximately 30 mL of absolute ethanol to afford 0.4 g of cyclohexanone 2,4-dinitrophenylhydrazone as orange flakes. The yield was 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384558B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-95e62093413b47619e906d83165283e4 |
| Source note | uspto-grants-2008_06 |