Methyl bromoacetate → HCID 22456961, compound
Reaction equation
[CH3:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH3:11])[CH:8]=2)[C:3]1=O.[CH3:13][O:14][C:15](=[O:18])[CH2:16]Br>>[CH3:1][C:2]1[CH2:10][C:9]2[C:4]([C:3]=1[CH2:16][C:15]([O:14][CH3:13])=[O:18])=[CH:5][CH:6]=[C:7]([CH3:11])[CH:8]=2Participants
3
Procedure
The above reactions of Example 13(C) are repeated except that the starting materials are 2,5-dimethylindanone and methylbromoacetate. Using the same reaction conditions and techniques there is obtained methyl 2,6-dimethyl-3-indenylacetate.
Workup
- customthe same reaction conditions and techniques
Sources & evidence
- ORD record
- ord-1e7ffea60cb74ffb966132b6ae8500ab
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06121321
Reaction notes
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