Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[N:6][C:7]=1[Cl:8].Br[CH:11]([CH2:16][CH3:17])[C:12]([O:14][CH3:15])=[O:13]>>[Cl:1][C:2]1[CH:3]=[C:4]([O:9][CH:11]([CH2:16][CH3:17])[C:12]([O:14][CH3:15])=[O:13])[CH:5]=[N:6][C:7]=1[Cl:8]Participants
3
Procedure
5,6-Dichloropyridin-3-ol was reacted with methyl 2-bromobutyrate using a similar procedure to that described in Example 1, Stage 1 to give methyl 2-(5,6-dichloro-3-pyridyloxy)butyrate, orange liquid.
Sources & evidence
- ORD record
- ord-7c233429af264149862e105014ccae21
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166621B2
Linked notes
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