1-(Difluoromethoxy)-4-iodobenzene → 5-(4-Difluoromethoxy-phenylethynyl)-2-methoxy-benzonitrile
Reaktionsgleichung
[F:1][CH:2]([F:11])[O:3][C:4]1[CH:9]=[CH:8][C:7](I)=[CH:6][CH:5]=1.[C:12]([C:14]1[CH:15]=[CH:16][C:17]([O:22][CH3:23])=[C:18]([CH:21]=1)[C:19]#[N:20])#[CH:13]>>[F:1][CH:2]([F:11])[O:3][C:4]1[CH:9]=[CH:8][C:7]([C:13]#[C:12][C:14]2[CH:15]=[CH:16][C:17]([O:22][CH3:23])=[C:18]([CH:21]=2)[C:19]#[N:20])=[CH:6][CH:5]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared in substantially the same manner as described in Example 12, step 3 starting from 1-Difluoromethoxy-4-iodo-benzene (0.17 g, 0.64 mmol), and 5-Ethynyl-2-methoxy-benzonitrile (0.10 g, 0.64 mmol), and was obtained as a light brown solid, (0.170 g, 89%), identified by NMR and mass spectral analyses. MS (APPI+): 299 (M+)
Aufarbeitung
- customwas obtained as a light brown solid, (0.170 g, 89%),
Quellen und Nachweise
- ORD-Eintrag
- ord-f71e8f4c937b4197a215fe3d80b3d720
- Quelldatensatz
- uspto-grants-2010_05
- Patentnummer
- US07723368B2
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