Aluminium lithium hydride → Benzofuran-6-ylmethanamine

HRID 911338Notes

Reaction equation

HRID 911338 reaction equation
[O:1]1[C:5]2[CH:6]=[C:7]([C:10]#[N:11])[CH:8]=[CH:9][C:4]=2[CH:3]=[CH:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[NH2:11][CH2:10][C:7]1[CH:8]=[CH:9][C:4]2[CH:3]=[CH:2][O:1][C:5]=2[CH:6]=1

Participants

4

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 212514851-Benzofuran-6-carbonitrile

Product 1

HCID 47002760Benzofuran-6-ylmethanamineYield 82.9%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
50 °C

Procedure

Dissolve benzofuran-6-carbonitrile (0.5 g, 3.28 mmol) in anhydrous THF (10 mL) and add slowly to 1M lithium aluminum hydride in THF (6.56 mL, 6.56 mmol) at ambient temperature. Heat the reaction mixture at 50° C. for 17 h and cool to ambient temperature. Quench the reaction mixture with water until a granular precipitate starts to form and filter through a pad of Celite®g. Evaporate the solvent and purify by SCX chromatography to obtain the title compound as a yellow oil (0.4 g, 79%).

Workup

  1. temperaturecool to ambient temperature
  2. customQuench the reaction mixture with water until a granular precipitate
  3. customto form
  4. filtrationfilter through a pad of Celite®g
  5. customEvaporate the solvent
  6. custompurify by SCX chromatography

Sources & evidence

ORD record
ord-c2d9fa380a5446d5a720d18f19dc641e
Source dataset
uspto-grants-2011_09
Patent number
US08022062B2

Reaction notes

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