Carbon Dioxide → 4-Cyclopropoxybenzoic acid

HRID 2068547

Reaktionsgleichung

Reaktionsgleichung von HRID 2068547
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH:9]2[CH2:11][CH2:10]2)=[CH:4][CH:3]=1.C([Li])CCC.CCCCCC.[C:23](=[O:25])=[O:24]>O1CCCC1>[CH:9]1([O:8][C:5]2[CH:6]=[CH:7][C:2]([C:23]([OH:25])=[O:24])=[CH:3][CH:4]=2)[CH2:11][CH2:10]1

Komponenten

6

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a −78° C. solution of 1-bromo-4-(cyclopropoxy)benzene (33 g, 154.9 mmol) in tetrahydrofuran (500 mL) add 1.6 M butyl lithium in hexane (96.8 mL, 154.9 mmol) while maintaining a temperature below −70° C. Stir the mixture at −78° C. for 20 minutes after the addition. Add dry ice (464.6 mmol) in 3 portions 5 minutes apart. Stir the mixture at −78° C. for 30 minutes. Remove the cooling bath and quench the mixture with 10% sodium hydrogen sulfate (NaHSO4) (200 mL). Warm the mixture to ambient temperature and extract 3× with EtOAc (300 mL). Combine the organics and wash once with brine, dry over sodium sulfate, filter, and concentrate under reduced pressure. Suspend the residue in diethyl ether and filter. Dry the solid in a vacuum oven to give the title compound (12.9 g, 47%): MS (m/z): 179 (M+1).

Aufarbeitung

  1. temperaturewhile maintaining a temperature below −70° C
  2. additionafter the addition
  3. customin 3 portions 5 minutes
  4. stirringStir the mixture at −78° C. for 30 minutes
  5. customRemove the cooling bath
  6. customquench the mixture with 10% sodium hydrogen sulfate (NaHSO4) (200 mL)
  7. temperatureWarm the mixture to ambient temperature
  8. extractionextract 3× with EtOAc (300 mL)
  9. washCombine the organics and wash once with brine
  10. dry with materialdry over sodium sulfate
  11. filtrationfilter
  12. concentrationconcentrate under reduced pressure
  13. filtrationfilter
  14. customDry the solid in a vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-7313c14a41944c09964968d8185c370e
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08299061B2

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