Aluminium lithium hydride → HCID 21355906, compound

HRID 566704Notes

Reaction equation

HRID 566704 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[NH2:7][C@@H:8]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C@H:9]([CH3:13])[C:10]([NH2:12])=O>O1CCCC1>[CH3:13][C@H:9]([CH2:10][NH2:12])[C@H:8]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[NH2:7]

Participants

4

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 54300456HCID 54300456, compound

Product 1

HCID 21355906HCID 21355906, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Lithium aluminium hydride (2.3 g, 60.60 mmol) was added in portions to a stirring solution of (2S,3R)-3-amino-2-methyl-3-phenylpropionamide (2.6 g, 14.59 mmol) in tetrahydrofuran (54 ml) at ice-bath temperature. After 45 min, the mixture was heated at reflux for 16 h. With ice-bath cooling, the reaction was quenched by the portionwise addition of sodium sulfate decahydrate and some methanol until hydrogen evolution ceased. The solids were removed by filtration and washed with dichloromethane. The combined filtrates were evaporated to provide the title compound. MS (m/z): 165.2 (M+H)+; C10H16N2 requir. 164.3.

Workup

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 16 h
  3. temperatureWith ice-bath cooling
  4. customthe reaction was quenched by the portionwise addition of sodium sulfate decahydrate
  5. customThe solids were removed by filtration
  6. washwashed with dichloromethane
  7. customThe combined filtrates were evaporated

Sources & evidence

ORD record
ord-b1142eba0d7a4d2bae9df31e0fb337a2
Source dataset
uspto-grants-2001_01
Patent number
US06174901B1

Reaction notes

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