4-(4-Chlorophenyl)butanamide → 4-(4-Chlorophenyl)butan-1-amine

HRID 510627Notes

Reaction equation

HRID 510627 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][C:17]([NH2:19])=O)=[CH:10][CH:9]=1>C(OCC)C.O1CCCC1>[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([CH2:14][CH2:15][CH2:16][CH2:17][NH2:19])=[CH:12][CH:13]=1

Participants

5

Reactant 2

HCID 110743574-(4-Chlorophenyl)butanamideHCID 21226445Aluminium lithium hydride

Product 1

HCID 107738224-(4-Chlorophenyl)butan-1-amineYield 61%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a stirred suspension of lithium aluminum hydride (1.84 g, 48.6 mmol) in diethyl ether (50 mL) at ambient temperature was added a solution of 4-(4-chlorophenyl)butanamide in tetrahydrofuran (25 mL), dropwise over 8 minutes. Stirring was continued at ambient temperature for a further 4 hours. The reaction mixture was carefully quenched by sequential slow addition of water (2 mL), 10M sodium hydroxide (0.75 mL), and water (7 mL). After stirring the mixture for 20 minutes, it was extracted with diethyl ether (50 mL). The organic layer was dried over sodium sulfate and concentrated to afford 4-(4-chlorophenyl)butan-1-amine as a light yellow oil (1.36 g, 61%).

Workup

  1. waitwas continued at ambient temperature for a further 4 hours
  2. customThe reaction mixture was carefully quenched by sequential slow addition of water (2 mL), 10M sodium hydroxide (0.75 mL), and water (7 mL)
  3. stirringAfter stirring the mixture for 20 minutes
  4. extractionit was extracted with diethyl ether (50 mL)
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-c58cc3f3fba747f983ac889d096599ce
Source dataset
uspto-grants-2015_08
Patent number
US09096567B2

Reaction notes

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