Hydride → 2-(1-Benzhydrylazetidin-3-YL)ethanamine

HRID 872

Reaction equation

HRID 872 reaction equation
[C:1]([CH2:3][CH:4]1[CH2:7][N:6]([CH:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:5]1)#[N:2].[H-].[H-].[H-].[H-].[Li+].[Al+3].[H-]>C1COCC1>[NH2:2][CH2:1][CH2:3][CH:4]1[CH2:7][N:6]([CH:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:5]1

Participants

5

Reactant 3

HCID 166653HydrideHCID 21226445Aluminium lithium hydrideHCID 222576333-Cyanomethyl-1-benzhydryl azetidine

Product 1

HCID 222576342-(1-Benzhydrylazetidin-3-YL)ethanamineYield 87%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

5.7 g (21.7 mmol) of 3-cyanomethyl-1-benzhydryl azetidine was added slowly to a suspension of 2.9 g (76.0 mmol) of LiAlH4 in 80 mL of dry THF at roomtemperature. The reaction mixture was refluxed for 4 h. Excess hydride reagent was hydrolyzed by careful addition, with cooling, of NH4 Cl(aq), the gelatinous mixture was filtered and the filter cake was washed repeatedly with THF. The solvent was evaporated, the residue was dissolved in diethyl ether, washed with brine and dried with Na2SO4. Evaporation of the solvent gave 5.0 g (87%) of the title compound.

Workup

  1. temperatureThe reaction mixture was refluxed for 4 h
  2. filtrationthe gelatinous mixture was filtered
  3. washthe filter cake was washed repeatedly with THF
  4. customThe solvent was evaporated
  5. dissolutionthe residue was dissolved in diethyl ether
  6. washwashed with brine
  7. dry with materialdried with Na2SO4
  8. customEvaporation of the solvent

Sources & evidence

ORD record
ord-df1a0a7ecbb7442b9ee9a9bf29ebf6f4
Source dataset
uspto-grants-1998_03
Patent number
US05723444

Linked notes

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