Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminobiphenyl | HCID 7015 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21955033 | HCID 21955033 | — |
| Product | HCID 178509175 | HCID 178509175 | 61% |
Reaction Steps
This compound was prepared using 123 mg (0.5 mmol) of 2-[(biphenyl-2-yl)hydrazono]-malononitrile, which was derived from 2-aminobiphenyl (169 mg, 1.0 mmol) and malononitrile (1.5 mmol) as described in Example 8, and hydrazine hydrate. Precipitate formed in the reaction tube immediately after the addition of the hydrazine hydrate then the solution cleared. Very little solid remained 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 85 mg (61%) of the title compound as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06436915B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-a1d8b578c6e14adeae11975db4f8c8aa |
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| Source note | uspto-grants-2002_08 |
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