Aluminium lithium hydride → HCID 69284532, compound
Reaction equation
C([O:3][C:4]([C:6]1[N:7]([CH3:20])[N:8]=[C:9]([C:13]2[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][CH:14]=2)[C:10]=1[CH2:11][CH3:12])=O)C.[H-].[Al+3].[Li+].[H-].[H-].[H-]>>[Cl:19][C:16]1[CH:15]=[CH:14][C:13]([C:9]2[C:10]([CH2:11][CH3:12])=[C:6]([CH2:4][OH:3])[N:7]([CH3:20])[N:8]=2)=[CH:18][CH:17]=1Participants
3
Procedure
In analogy to the procedure described for example 1 a], 5-(4-chloro-phenyl)-4-ethyl-2-methyl-2H-pyrazole-3-carboxylic acid ethyl ester was reduced with lithium aluminium hydride to give [5-(4-chloro-phenyl)-4-ethyl-2-methyl-2H-pyrazol-3-yl]-methanol as colorless crystals.
Sources & evidence
- ORD record
- ord-e5b7015803b347cda726b098be213ea9
- Source dataset
- uspto-grants-2007_09
- Patent number
- US07265149B2
Reaction notes
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