(4-Bromophenyl)boronic acid → Ethyl 6-(4-bromophenyl)nicotinate
Reaktionsgleichung
Br[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][N:3]=1.[Br:13][C:14]1[CH:19]=[CH:18][C:17](B(O)O)=[CH:16][CH:15]=1>>[Br:13][C:14]1[CH:19]=[CH:18][C:17]([C:2]2[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][N:3]=2)=[CH:16][CH:15]=1Komponenten
3
Versuchsvorschrift
In accordance with Example 11-(1), but using ethyl 6-bromonicotinate instead of 4-bromobenzylbromide, and 4-bromophenylboronic acid instead of [3-(hydroxymethyl)phenyl]boronic acid, the title compound (yield 98%) was afforded as a white solid.
Quellen und Nachweise
- ORD-Eintrag
- ord-ed36ab0287a34f0ca47e1ec93bfc6434
- Quelldatensatz
- uspto-grants-2014_07
- Patentnummer
- US08785462B2
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