HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile → HCID 178493283, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 5-(Trifluoromethyl)-m-anisidine | HCID 605671 | — |
| Reactant | HCID 21954979 | HCID 21954979 | — |
| Product | HCID 178493283 | HCID 178493283 | 7% |
Reaction Steps
This compound was prepared using 134 mg (0.5 mmol) of 2-[(3-methoxy-5-trifluoromethylphenyl)hydrazono]malononitrile, which was derived from 3-methoxy-5-trifluoromethylaniline (191 mg, 1.0 mmol) and malononitrile (1.5 mmol) as described in Example 8, and hydrazine hydrate. Very little solid had formed after heating the reaction at 75° C. for 1 hr, however, analysis of the reaction solution by TLC indicated that no starting material remained. The solution was allowed to cool to room temperature and the solvent was evaporated. The residue was dissolved in ethyl acetate and then precipitated by the addition of hexanes. The resulting solid was isolated by filtration and dried to yield 10 mg (7%) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436915B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-c34cf1fb5fcc4a0098f31f6faa6f3e69 |
| Source note | uspto-grants-2002_08 |