Water → [(1-Benzylpyrrolidin-3-yl)methyl](2,2,2-trifluoroethyl)amine

HRID 980707Notes

Reaction equation

HRID 980707 reaction equation
O=[C:2]1[N:6]([CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:5][CH:4]([CH2:14][NH:15][CH2:16][C:17]([F:20])([F:19])[F:18])[CH2:3]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[C:8]1([CH2:7][N:6]2[CH2:2][CH2:3][CH:4]([CH2:14][NH:15][CH2:16][C:17]([F:20])([F:18])[F:19])[CH2:5]2)[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1

Participants

6

Procedure

A mixture of 8.50 g (28.3 mole) of 5-oxo-1-(phenylmethyl)-N-(2,2,2-trifluoroethyl)-3-pyrrolidinemethanamine in 100 ml tetrahydrofuran was added dropwise to 3.22 g (84.9 mmole) of lithium aluminum hydride in 50 ml tetrahydrofuran. The reaction was refluxed two hours, then stirred at room temperature overnight. The reaction was cooled in an ice bath and 3.2 ml of water, 3.2 ml of 15% sodium hydroxide, and 9.6 ml of water were added. The precipitated salts were filtered and washed with hot ethanol. The combined filtrates were concentrated under reduced pressure. The residue was taken up in dichloromethane, filtered, and dried over magnesium sulfate. The solvent was removed at reduced pressure to give 7.15 g of 1-(phenylmethyl-N-(2,2,2-trifluoroethyl)-3-pyrrolidinemethanamine.

Workup

  1. temperatureThe reaction was refluxed two hours
  2. temperatureThe reaction was cooled in an ice bath
  3. filtrationThe precipitated salts were filtered
  4. washwashed with hot ethanol
  5. concentrationThe combined filtrates were concentrated under reduced pressure
  6. filtrationfiltered
  7. dry with materialdried over magnesium sulfate
  8. customThe solvent was removed at reduced pressure

Sources & evidence

ORD record
ord-e5dea57cb4074359a2eb0ece00eef89f
Source dataset
uspto-grants-1987_01
Patent number
US04638067

Reaction notes

Loading…