HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (1-Benzyl-pyrrolidin-3-ylmethyl)-ethyl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-ethyl-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide | HCID 13491793 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Benzyl-pyrrolidin-3-ylmethyl)-ethyl-amine | HCID 5127972 | 88.1% |
Reaction Steps
To a suspension of 108.68 g (2.860 mole) lithium aluminum hydride in 800 ml tetrahydrofuran, was added a solution of 194.5 g (0.790 mole) of N-ethyl-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide in 600 ml tetrahydrofuran dropwise under nitrogen. The reaction was then refluxed four hours. The reaction flask was cooled in an ice bath and 108 ml of water, 108 ml of 15% sodium hydroxide, and 324 ml of water were added. The precipitated solids were filtered and washed with hot ethanol. The combined filtrates were concentrated, then dissolved in dichloromethane, filtered, dried over magnesium sulfate, and the solvent evaporated under reduced pressure to give 151.9 g of N-ethyl-1-(phenylmethyl)-3-pyrrolidinemethanamine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04604401 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-33f83bc72b294eddb430c59228b45754 |
| Source note | uspto-grants-1986_08 |