HuagongsheHuagongshe Chemistry Print Report · For research reference only
Malononitrile → HCID 178509173, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 4199189 | HCID 4199189 | — |
| Product | HCID 178509173 | HCID 178509173 | 66% |
Reaction Steps
This compound was prepared using 125 mg (0.5 mmol) of 2-[(3-bromophenyl)-hydrazono]malononitrile, which was derived from 3-bromoaniline (172 mg, 1.0 mmol) and malononitrile (1.5 mmol) as. described in Example 8, and hydrazine hydrate. The hydrazine hydrate was added to the solution at a temperature of 75° C. despite the fact that the starting material had not fully dissolved. The solution cleared briefly and then a precipitate formed. The resulting solid was isolated by filtration, washed with ethanol, and dried to yield 93 mg (66%) of the title compound as an orange solid. 1H NMR (ppm, DMSO-d6): 6.2 (br s, 4H), 7.21-7.32 (m, 2H), 7.50-7.62 (m, 1H), 7.90 (s, 1H), 10.71 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436915B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-da9b3b1aece94cf196be01260d774b22 |
| Source note | uspto-grants-2002_08 |