4-Fluorobenzaldehyde → Methyl 4-(4-fluorophenyl)-5-(hydroxymethyl)-2,6-di(propan-2-yl)pyridine-3-carboxylate
Reaction equation
[C:1]([CH2:6][C:7]([O:9][CH3:10])=[O:8])(=O)[CH:2]([CH3:4])[CH3:3].[F:11][C:12]1[CH:19]=[CH:18][C:15]([CH:16]=O)=[CH:14][CH:13]=1.[C:20]([O-:23])(=O)[CH3:21].[NH4+:24]>>[CH:2]([C:1]1[C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:16]([C:15]2[CH:18]=[CH:19][C:12]([F:11])=[CH:13][CH:14]=2)[C:21]([CH2:20][OH:23])=[C:1]([CH:2]([CH3:4])[CH3:3])[N:24]=1)([CH3:4])[CH3:3]Participants
4
Procedure
Prepared from methyl isobutyrylacetate, 4-fluorobenzaldehyde and ammonium acetate by the procedures described in Example 1, Steps A-D.
Sources & evidence
- ORD record
- ord-dcbb50dafd034dc29239faca6dcaf9ea
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06218431B1
Reaction notes
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