Tributylphosphine → 2-(3-(4-Bromophenyl)propoxy)-3-chloro-1,4-difluorobenzene
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][OH:11])=[CH:4][CH:3]=1.[Cl:12][C:13]1[C:18]([F:19])=[CH:17][CH:16]=[C:15]([F:20])[C:14]=1O.N(C(N1CCCCC1)=O)=NC(N1CCCCC1)=O.C(P(CCCC)CCCC)CCC>CCOCC.C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][O:11][C:14]2[C:13]([Cl:12])=[C:18]([F:19])[CH:17]=[CH:16][C:15]=2[F:20])=[CH:6][CH:7]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
3-(4-Bromophenyl)propan-1-ol from the previous step (1 eq.) and 2-chloro-3,6-difluorophenol (1 eq.) were taken up in freshly deoxygenated toluene (0.3 M). To this solution was then added 1,1′-(azodicarbonyl)-dipiperidine (1.2 eq.) and finally tributylphosphine (1.2 eq.). The resulting yellow solution was heated at 80° C. for 2 h. The reaction mixture was cooled to RT, diluted with ether, and washed with 1 N aq. NaOH. The aqueous wash was back extracted with ether and the combined organic extracts were dried over MgSO4. Filtration and concentration of the filtrate in vacuo afforded a yellow semi-solid. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→15:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.
Aufarbeitung
- temperatureThe reaction mixture was cooled to RT
- washwashed with 1 N aq. NaOH
- washThe aqueous wash
- extractionwas back extracted with ether
- dry with materialthe combined organic extracts were dried over MgSO4
- filtrationFiltration and concentration of the filtrate in vacuo
- customafforded a yellow semi-solid
- customPurification of the crude product
- customthus obtained by way of flash chromatography (SiO2, Hex→15:1 (v/v) Hex:EtOAc)
Quellen und Nachweise
- ORD-Eintrag
- ord-3113e977140649649adde3ee3d4a5b46
- Quelldatensatz
- uspto-grants-2011_11
- Patentnummer
- US08063105B2
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