6-Phenoxy-2-pyridinemethanol → HCID 54515175, compound
Reaction equation
[CH:1]([CH:4]([CH:8]=[C:9]([Cl:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:5]([OH:7])=[O:6])([CH3:3])[CH3:2].[O:17]([C:24]1[N:29]=[C:28]([CH2:30]O)[CH:27]=[CH:26][CH:25]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[CH:1]([CH:4]([CH:8]=[C:9]([Cl:16])[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)[C:5]([O:7][CH2:30][C:28]1[CH:27]=[CH:26][CH:25]=[C:24]([O:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[N:29]=1)=[O:6])([CH3:3])[CH3:2]Participants
3
Procedure
The acid chloride of 2-isopropyl-4-chloro-4-phenyl-3-butenoic acid is reacted with (6-phenoxy-2-pyridyl)methanol using the procedure of Example 1 to give (6-phenoxy-2-pyridyl)methyl 2-isopropyl-4-chloro-4-phenyl-3-butenoate.
Sources & evidence
- ORD record
- ord-8ad041202433456da3ad464109b0b69b
- Source dataset
- uspto-grants-1981_02
- Patent number
- US04248875
Reaction notes
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