Ethyl bromoacetate → Ethyl 2-(4-chloro-2-methoxyphenoxy)acetate
Reaction equation
Br[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[C:11]([O:16][CH3:17])[CH:10]=1>>[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])=[C:11]([O:16][CH3:17])[CH:10]=1Participants
3
Procedure
The subtitle compound was prepared by the method of example 1 step (iv) using ethyl bromoacetate and 4-chloro-2-methoxyphenol Yield 2.7 g
Sources & evidence
- ORD record
- ord-d35a8cc215e14608b6def6ec128faa15
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08394986B2
Reaction notes
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