Tetrahydrofurfuryl alcohol → 6-((Tetrahydrofuran-2-yl)methoxy)-5-(trifluoromethyl)picolinic acid
Reaktionsgleichung
Cl[C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[CH:4][C:3]=1[C:11]([F:14])([F:13])[F:12].[O:15]1[CH2:19][CH2:18][CH2:17][CH:16]1[CH2:20][OH:21]>>[O:15]1[CH2:19][CH2:18][CH2:17][CH:16]1[CH2:20][O:21][C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[CH:4][C:3]=1[C:11]([F:14])([F:13])[F:12]Komponenten
3
Versuchsvorschrift
The title compound was prepared in analogy to the procedure described in Example 230 b), using 6-chloro-5-(trifluoromethyl)picolinic acid and (tetrahydrofuran-2-yl)methanol (CAN 97-99-4) as starting materials. MS: 290.0 [M−H]−.
Quellen und Nachweise
- ORD-Eintrag
- ord-8d67f38cd1094190b45a8d908d1bb9c4
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09290451B2
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