HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-(Methylenedioxy)phenylacetonitrile → 2-(alpha-Cyano-3,4-methylenedioxybenzylidene)-1-methylpyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-(Methylenedioxy)phenylacetonitrile | HCID 78178 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Dimethylamino-1-methyl-1-pyrrolinium methylsulfate | HCID 178483037 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(alpha-Cyano-3,4-methylenedioxybenzylidene)-1-methylpyrrolidine | HCID 54151202 | — |
Reaction Steps
Add (dropwise at 80°, with stirring) a solution of 3.5 g of sodium in 80 ml of ethanol to a mixture of 16.1 g of 3,4-methylenedioxybenzylcyanide and 36 g of 2-dimethylamino-1-methyl-1-pyrrolinium-methylsulfate. Continue boiling the resulting reaction mixture for a further 2 hours. Then distil off the solvent under a vacuum and take up the residue with water/diethyl ether. Collect the ethereal layer. Dry it over sodium sulfate and concentrate it to obtain 18 g (67% of theory) of the title compound as oily liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04279918 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-e4dd16b6213b467da7fe405c831f3ce1 |
| Source note | uspto-grants-1981_07 |