Methyl bromoacetate → HCID 21539951, compound

HRID 1076342Notes

Reaction equation

HRID 1076342 reaction equation
[CH3:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:11]#[N:12])[CH:8]=2)[C:3]1=O.[CH3:14][O:15][C:16](=[O:19])[CH2:17]Br>>[CH3:1][C:2]1[CH2:10][C:9]2[C:4]([C:3]=1[CH2:17][C:16]([O:15][CH3:14])=[O:19])=[CH:5][CH:6]=[C:7]([C:11]#[N:12])[CH:8]=2

Participants

3

Reactant 2

HCID 60984Methyl bromoacetateHCID 14853009HCID 14853009, compound

Product 1

HCID 21539951HCID 21539951, compound

Procedure

The above reactions of Example 1C are repeated except that the starting materials are 2-methyl-5-cyanoindanone and methylbromoacetate. Using the same reaction conditions and techniques there is obtained methyl 2-methyl-6-cyano-3-indenylacetate.

Workup

  1. customthe same reaction conditions and techniques

Sources & evidence

ORD record
ord-f9a93b99796a40a1878f1b852fb8fcd5
Source dataset
uspto-grants-1976_05
Patent number
US03956363

Reaction notes

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