HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Phenylmethyl)hydrazine → 5-amino-1-benzyl-1H-pyrazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Phenylmethyl)hydrazine | HCID 11157 | — |
| Reactant | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-amino-1-benzyl-1H-pyrazole-4-carbonitrile | HCID 660147 | — |
Reaction Steps
A procedure analogous to that described in Example 1 was followed except 1.55 g (12.7 mM) of ethoxymethylene malononitrile was added to 1.70 g (13.9 mM) of benzylhydrazine in ethanol. Following completion of the reaction 0.82 g (33%) of the product was obtained as a tan solid; tlc, Rf =0.24, silica gel, ethyl acetate:hexane (1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04546104 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-cb0f671da4b8429eacbd05ddb6ba7e30 |
| Source note | uspto-grants-1985_10 |