HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 3-Amino-1-benzylpyrrolidine-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Benzyl-3-pyrrolidinone | HCID 69890 | — |
| Product | 3-Amino-1-benzylpyrrolidine-3-carbonitrile | HCID 22063369 | — |
Reaction Steps
According to a particular variant of embodiment of this synthesis process, 1-benzyl-3-pyrrolidinone is treated with an ammoniacal solution of ammonium chloride and of potassium cyanide to obtain (±)-3-amino-1-benzyl-3-cyanopyrrolidine. This compound is then converted by acid or basic hydrolysis to (±)-3-amino-1-benzyl-3-pyrrolidinecarboxylic acid, and lastly a reduction with hydrogen, preferably a catalytic hydrogenolysis, is carried out to obtain (±)-3-amino-3-pyrrolidinecarboxylic acid or (±)-cucurbitine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05653997 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-f03766eee2514b9cbdaed4616e669b88 |
| Source note | uspto-grants-1997_08 |