Aluminium lithium hydride → HCID 21260549, compound

HRID 634783Notes

Reaction equation

HRID 634783 reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][CH:18]([NH:21][C:22](=O)[CH2:23][CH2:24][CH2:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[CH2:17][CH2:16]2)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][CH:18]([NH:21][CH2:22][CH2:23][CH2:24][CH2:25][C:26]3[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=3)[CH2:17][CH2:16]2)=[CH:11][CH:10]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 21226445Aluminium lithium hydrideHCID 21260498HCID 21260498, compound

Product 1

HCID 21260549HCID 21260549, compoundYield 17.2%

Procedure

Following the procedure of example 40b, N-[1-(4-benzyloxy-phenyl)-piperidin-4-yl]-4-phenyl-butyramide (450 mg) was reduced with LiAlH4 to give [1-(4-benzyloxy-phenyl)-piperidin-4-yl]-(4-phenyl-butyl)-amine (75 mg; 17%) as a light yellow solid (MS: m/e=415.4 (M+H+)).

Sources & evidence

ORD record
ord-88c04ee563ee4a689f96c36313bfe48d
Source dataset
uspto-grants-2001_02
Patent number
US06184236B2

Reaction notes

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