HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzyl cyanide → 2-(alpha-Cyano-4-chlorobenzylidene)-1-methylpyrrolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzyl cyanide | HCID 241582 | — |
| Reactant | 2,2-Diethoxy-1-methylpyrrolidine | HCID 297308 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(alpha-Cyano-4-chlorobenzylidene)-1-methylpyrrolidine | HCID 53867175 | — |
Reaction Steps
Boil 22.7 g of 2,2-diethoxy-1-methylpyrrolidine, 19.8 g of 4-chlorobenzylcyanide and 90 ml of benzene for 1 hour under reflux and with stirring. Distil off the volatile constituents under a vacuum. After trituration with a little diethyl ether, filter off the residue to obtain 20.8 g (68% of theory) and the title compound (m.p. 71° to 72° from isopropanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04279918 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-38d157ccb44247ad82d5a58cc7c67f0b |
| Source note | uspto-grants-1981_07 |