2',4'-Bis(trifluoromethyl)acetophenone → 2,4-Bis(trifluoromethyl)phenacyl bromide
Reaktionsgleichung
[F:1][C:2]([F:17])([F:16])[C:3]1[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=[CH:5][C:4]=1[C:13](=[O:15])[CH3:14].[Br:18]CC(C1C=C(Cl)C=CC=1Cl)=O>>[F:1][C:2]([F:16])([F:17])[C:3]1[CH:8]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:6]=[CH:5][C:4]=1[C:13](=[O:15])[CH2:14][Br:18]Komponenten
3
Versuchsvorschrift
This compound was prepared from 1-[2,4-bis(trifluoromethyl)phenyl]ethanone (5.0 g, 19.52 mmol) in the manner described for 2-bromo-1-(2,5-dichlorophenyl)ethanone, affording 4.12 g (63%) of a white solid. 1H-NMR (DMSO-d6) δ 8.28 to 8.16 (m, 3H), 4.98 (s, 2H);
Quellen und Nachweise
- ORD-Eintrag
- ord-d4e6157071314c318953affbad42f9e0
- Quelldatensatz
- uspto-grants-2008_06
- Patentnummer
- US07384947B2
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