Sodium Hydroxide → (2E,4E,6E)-6-Fluoro-7-(4-isopropyl-7-methoxy-2,2-dimethyl-2H-chromen-6-yl)-3-methyl-octa-2,4,6-trienoic acid
Reaktionsgleichung
[F:1]/[C:2](=[C:13](/[C:15]1[CH:16]=[C:17]2[C:22](=[CH:23][C:24]=1[O:25][CH3:26])[O:21][C:20]([CH3:28])([CH3:27])[CH:19]=[C:18]2[CH:29]([CH3:31])[CH3:30])\[CH3:14])/[CH:3]=[CH:4]/[C:5](/[CH3:12])=[CH:6]/[C:7]([O:9]CC)=[O:8].[OH-].[Na+]>C(O)C.C1COCC1>[F:1]/[C:2](=[C:13](/[C:15]1[CH:16]=[C:17]2[C:22](=[CH:23][C:24]=1[O:25][CH3:26])[O:21][C:20]([CH3:28])([CH3:27])[CH:19]=[C:18]2[CH:29]([CH3:31])[CH3:30])\[CH3:14])/[CH:3]=[CH:4]/[C:5](/[CH3:12])=[CH:6]/[C:7]([OH:9])=[O:8]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Following General Procedure G, a solution of ethyl (2E,4E,6E)-6-fluoro-7-(4-isopropyl-7-methoxy-2,2-dimethyl-2H-chromen-6-yl)-3-methyl-octa-2,4,6-trienoate (Compound 108, 116 mg, 2.71 mmol) in ethanol and THF was hydrolyzed with NaOH to yield a yellow oil after purification by column chromatography (silica gel, 100% hexane to 5% to 50% ethyl acetate in hexanesethyl). The resulting oil was recrystallized from acetonitrile to produce the title compound as a yellow solid.
Aufarbeitung
- customto yield a yellow oil
- customafter purification by column chromatography (silica gel, 100% hexane to 5% to 50% ethyl acetate in hexanesethyl)
- customThe resulting oil was recrystallized from acetonitrile
Quellen und Nachweise
- ORD-Eintrag
- ord-a2de77370f3c49598edc7cf64392abb3
- Quelldatensatz
- uspto-grants-2005_05
- Patentnummer
- US06887896B1
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