HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → Hydrazinecarboxaldehyde, 2-(4-nitrophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | (4-Nitrophenyl)hydrazine | HCID 3310889 | — |
| Product | Hydrazinecarboxaldehyde, 2-(4-nitrophenyl)- | HCID 5008489 | 91.2% |
Reaction Steps
Then, 1-formyl-2-(4-aminophenyl)hydrazide was synthesized according to the process described in Japanese Patent Application (OPI) No. 74729/79. Namely, to 1.6 l of acetonitrile, 459 g of 4-nitrophenylhydrazine was added with stirring, and 322 g of formic acid was then gradually added thereto to obtain a homogeneous solution. After 20 minutes, crystals were deposited. After carried out the reaction at a temperature of 80° C. for further 2 hours, the mixture was cooled and filtered to separate crystals. The crystals were washed with acetonitrile and dried to obtain 495 g of 1-formyl-2-(4-nitrophenyl)hydrazine. Melting Point: 184° to 186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04628024 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-b1839bb3ad7e497d90750e928cc5accb |
| Source note | uspto-grants-1986_12 |