HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Nitrophenylacetonitrile → 2-(alpha-Cyano-4-nitrobenzylidene)-1-methylpyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Nitrophenylacetonitrile | HCID 68386 | — |
| Reactant | 2,2-Diethoxy-1-methylpyrrolidine | HCID 297308 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(alpha-Cyano-4-nitrobenzylidene)-1-methylpyrrolidine | HCID 54437636 | — |
Reaction Steps
Stir 29.9 g of 2,2-diethoxy-1-methylpyrrolidine and 28 g of 4-nitrophenylacetonitrile in 80 ml of benzene for one hour at room temperature. Distil off the solvent from the resulting reaction mixture under a vacuum to produce a crystalline residue. Recrystallize this residue from ethanol/diethyl ether. Concentrate the mother liquor to obtain a total of 29.5 g (70% of theory) of the title compound as dark-brown shiny crystals of m.p. 67°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04279918 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-2286baadb1cf47f48bddfcc51e136d07 |
| Source note | uspto-grants-1981_07 |