Azobisisobutyronitrile → Ethyl o-bromomethylphenylacetate
Reaktionsgleichung
[C:1]1([CH3:11])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8]([OH:10])=[O:9].C1C(=O)N([Br:19])C(=O)C1.CC(N=N[C:27]([C:30]#N)(C)C)(C#N)C>>[Br:19][CH2:11][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][C:8]([O:10][CH2:27][CH3:30])=[O:9]Komponenten
4
Versuchsvorschrift
o-Tolylacetic acid was brominated with NBS and AIBN as described in Example 21 to give ethyl o-bromomethylphenylacetate, and this was reacted with triethyl phosphite as described in Example 2.
Quellen und Nachweise
- ORD-Eintrag
- ord-67807ba4f6aa49a6bfa5666d55bc49c7
- Quelldatensatz
- uspto-grants-1993_09
- Patentnummer
- US05242908
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