HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2,4-Dichlorobenzylidenemalononitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | 2,4-Dichlorobenzaldehyde | HCID 13404 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 2,4-Dichlorobenzylidenemalononitrile | HCID 18089 | — |
Reaction Steps
Under an atmosphere of argon, 2,4-dichlorobenzaldehyde (30.00 g, 171 mmol) and malononitrile (13.59 g, 206 mmol) were suspended in 1-butanol (350 ml). After stirring for 15 min, 8 drops of piperidine were added at room temperature. After stirring for an additional 3 h, diethyl ether was added. The precipitate was filtered and washed with diethyl ether and hexane to give the title compound, MS: m/e=222.8 (M+), as a colorless solid (35.34 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07022718B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-c7465b18f3304bd997cf59174ec964ad |
| Source note | uspto-grants-2006_04 |