HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 20319374, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Hydrazinecarboxamide, 1-phenyl- | HCID 170220 | — |
| Reactant | 1-(3-Chloro-4-fluorophenyl)-N,N-dimethylhydrazine-1-carboxamide | HCID 12789936 | — |
| Reactant | HCID 54519082 | HCID 54519082 | — |
| Reactant | HCID 70621649 | HCID 70621649 | — |
| Product | HCID 20319374 | HCID 20319374 | — |
Reaction Steps
A suitable method for preparing the 2-phenylsemicarbazones comprises converting a 2-phenylsemicarbazone of one specific aldehyde into a 2-phenyl-semicarbazone of a different aldehyde by hydrolyzing the initially prepared 2-phenylsemicarbazone into the corresponding 2-phenylsemicarbazide which is then reacted with the desired aldehyde. For example, benzaldehyde 2-(3-chloro-4-fluorophenyl)-4,4-dimethylsemicarbazone prepared e.g., from benzaldehyde 3-chloro-4-fluorophenylhydrazone and dimethylcarbamoyl chloride is hydrolyzed to 2-(3-chloro-4-fluorophenyl)-4,4-dimethylsemicarbazide which is reacted with formaldehyde to give formaldehyde 2-(3-chloro-4-fluorophenyl)-4,4-dimethylsemicarbazone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04099956 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-d901976963b54d30a2e0048aa6a6af04 |
| Source note | uspto-grants-1978_07 |