Reaktionsgleichung
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([CH:15]([OH:20])[CH2:16][CH2:17][CH2:18][CH3:19])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.P(CCCC)(CCCC)CCCC.O[C:37]1[CH:49]=[CH:48][C:40]([O:41][CH2:42][C:43]([O:45][CH2:46][CH3:47])=[O:44])=[C:39]([CH3:50])[CH:38]=1>C1COCC1>[CH3:50][C:39]1[CH:38]=[C:37]([O:20][CH:15]([C:12]2[CH:13]=[CH:14][C:9]([C:6]3[CH:5]=[CH:4][C:3]([C:2]([F:21])([F:22])[F:1])=[CH:8][CH:7]=3)=[CH:10][CH:11]=2)[CH2:16][CH2:17][CH2:18][CH3:19])[CH:49]=[CH:48][C:40]=1[O:41][CH2:42][C:43]([O:45][CH2:46][CH3:47])=[O:44]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 1-[4′-(trifluoromethyl)-4-biphenylyl]-1-pentanol (250 mg, 0.81 mmol) in dry THF (20 mL) under nitrogen at 0° C. (ice/water bath) was added nBu3P (0.41 mL, 1.64 mmol), followed by ethyl (4-hydroxy-2-methylphenoxy)acetate (170 mg, 0.81 mmol) and ADDM (420 mg, 1.64 mmol) portion-wise. After stirring the mixture for 18 hours at rt under nitrogen the solvent was removed under vacuum. The residue was partitioned between water and EtOAc and the aqueous re-extracted with EtOAc (3×30 mL). The organic combined extract was dried (MgSO4) and then reduced under vacuum. Purification by flash chromatography (silica), eluting with cyclohexane:EtOAc (9:1) afforded the title compound as a colourless gum (310 mg).
Aufarbeitung
- customwas removed under vacuum
- customThe residue was partitioned between water and EtOAc
- extractionthe aqueous re-extracted with EtOAc (3×30 mL)
- extractionThe organic combined extract
- dry with materialwas dried (MgSO4)
- customPurification by flash chromatography (silica)
- washeluting with cyclohexane:EtOAc (9:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-120236c456054dc093758b5e3d8d6422
- Quelldatensatz
- uspto-grants-2008_03
- Patentnummer
- US07338960B2
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