Water → 1-(phenylmethyl)-N-propyl-3-pyrrolidinemethanamine

HRID 2372051Notes

Reaction equation

HRID 2372051 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].O=[C:8]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:11][CH:10]([C:20]([NH:22][CH2:23][CH2:24][CH3:25])=O)[CH2:9]1.O.[OH-].[Na+]>O1CCCC1>[C:14]1([CH2:13][N:12]2[CH2:8][CH2:9][CH:10]([CH2:20][NH:22][CH2:23][CH2:24][CH3:25])[CH2:11]2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1

Participants

6

Procedure

To a suspension of 8.2 g (0.2 mole) of lithium aluminum hydride in 150 ml of dry tetrahydrofuran was added portionwise, 12.0 g (45.6 mmole) of solid 5-oxo-1-(phenylmethyl)-N-propyl-3-pyrrolidinecarboxamide. When the addition was complete, the reaction mixture was stirred at room temperature for 18 hours and then at reflux for two hours. After cooling to room temperature, the mixture was treated dropwise, successively, with 8 ml of water, 8 ml of 15% aqueous sodium hydroxide and 24 ml of water, titrating the final addition to produce a granular precipitate. The solid was removed by filtration, washed with tetrahydrofuran and the filtrate evaporated in vacuo to give 9.6 g of 1-(phenylmethyl)-N-propyl-3-pyrrolidinemethanamine, as a heavy syrup.

Workup

  1. additionwas added portionwise
  2. additionWhen the addition
  3. temperatureat reflux for two hours
  4. temperatureAfter cooling to room temperature
  5. additionthe mixture was treated dropwise
  6. additionaddition
  7. customto produce a granular precipitate
  8. customThe solid was removed by filtration
  9. washwashed with tetrahydrofuran
  10. customthe filtrate evaporated in vacuo

Sources & evidence

ORD record
ord-30eee712f0734f22ace1dd66aa5ed0e8
Source dataset
uspto-grants-1992_03
Patent number
US05097032

Reaction notes

Loading…