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 1C are repeated except that the starting materials are 2,5-dimethylindanone and methylbromoacetate. With the same reaction conditions and techniques, methyl 2,6-dimethyl-3-indenylacetate is obtained.
Workup
- customWith the same reaction conditions and techniques
Sources & evidence
- ORD record
- ord-9bb9bdf87e284ef3af83c959815d1b55
- Source dataset
- uspto-grants-1995_03
- Patent number
- US05401774
Reaction notes
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