Carbon Dioxide → 5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid

HRID 1003785Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1003785
C1O[C:4]2([CH2:13][CH2:12][C:11]3[C:6](=[CH:7][CH:8]=[C:9](Br)[CH:10]=3)[CH2:5]2)OC1.C([Li])(C)(C)C.[C:21](=[O:23])=[O:22].C1C[O:27]CC1>>[C:5]1(=[O:27])[C:6]2[C:11](=[CH:10][C:9]([C:21]([OH:23])=[O:22])=[CH:8][CH:7]=2)[CH2:12][CH2:13][CH2:4]1

Komponenten

5

Edukt 4

HCID 280Carbon DioxideHCID 8028TetrahydrofuranHCID 233778946-Bromo-2-tetralone ethylene ketalHCID 178418306HCID 178418306, Verbindung

Produkt 1

HCID 28184935-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

6-Bromo-2-tetralone ethylene ketal (2.2 g, 8.15 mmol) was dissolved in anhydrous THF (30 mL), cooled to -78° C. and treated with tert-butyllithium (12.05 mL, 20.4 mmol, 1.7M in pentane) under an atmosphere of nitrogen. After stirring for 30 minutes, anhydrous carbon dioxide gas was passed through the reaction mixture for 20 minutes at -78° C. The suspension was then allowed to warm to ambient temperature. The solution was quenched with water and acidified with 1N HCl, then extracted 2×EtOAc. The organic extracts were washed with brine, dried over Na2SO4 and concentrated in vacuo to a pale brown oil. The oily residue was applied to a silica flash chromatography column and eluted with 30%-50% EtOAC in hexanes to yield Tetralone-6-carboxylic acid, ethylene ketal 1.06 g (55%) of a slowly crystallizing solid. NMR. MS.

Aufarbeitung

  1. temperatureto warm to ambient temperature
  2. customThe solution was quenched with water
  3. extractionextracted 2×EtOAc
  4. washThe organic extracts were washed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo to a pale brown oil
  7. washeluted with 30%-50% EtOAC in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-00b2415dafc9492e8f80f27eafb3aea0
Quelldatensatz
uspto-grants-2000_04
Patentnummer
US06046227

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