lithium aluminium hydride THF → [4-(3,4-Dichlorophenyl)-2-pyridinyl]methanol
Reaction equation
C[O:2][C:3]([C:5]1[CH:10]=[C:9]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([Cl:18])[CH:12]=2)[CH:8]=[CH:7][N:6]=1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].C1COCC1>C1COCC1>[Cl:18][C:13]1[CH:12]=[C:11]([C:9]2[CH:8]=[CH:7][N:6]=[C:5]([CH2:3][OH:2])[CH:10]=2)[CH:16]=[CH:15][C:14]=1[Cl:17]Participants
4
Procedure
The title compound, MS: m/e=252.0 ([M−H]−) was obtained as a light brown oil (94% yield) by the reaction of 4-(3,4-dichloro-phenyl)-pyridine-2-carboxylic acid methyl ester with 1M lithium aluminum hydride/THF solution in THF at 20° C. for 1 h followed by chromatographic purification.
Sources & evidence
- ORD record
- ord-b309bc0be4c84e2abb550bfa712706bc
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683097B2
Reaction notes
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