Water → 3,3-Dimethyl-2,3-dihydro-1-benzofuran

HRID 460304Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 460304
Br[C:2]1[CH:3]=[CH:4][C:5]2[O:9][CH2:8][C:7]([CH3:11])([CH3:10])[C:6]=2[CH:12]=1.C([Li])CCC.CCCCCC.O>O1CCCC1>[CH3:10][C:7]1([CH3:11])[C:6]2[CH:12]=[CH:2][CH:3]=[CH:4][C:5]=2[O:9][CH2:8]1

Komponenten

6

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

To a solution of 5-bromo-3,3-dimethyl-2,3-dihydro-benzofuran (example 1f) (3.3 g, 14.53 mmol) in tetrahydrofuran (30 mL) was added dropwise, at −78° C., under an atmosphere of argon, a solution of n-butyllithium in hexane (8.8 mL, 22 mmol). The mixture was stirred at −78° C. for 5 minutes, then water was added and the mixture was warmed up to room temperature and stirred for 30 minutes. The layers were separated. The aqueous layer was extracted twice with ethyl acetate and the organic combined extract was washed with water, brine, dried (MgSO4), and filtered. The solvent was evaporated to afford 2.13 g of 3,3-dimethyl-2,3-dihydro-benzofuran. 99% yield. 1H-NMR (300 MHz, CDCl3): 1.35 (s, 6H), 4.23 (s, 2H), 6.79 (d, J=7.6 Hz, 1H), 6.88 (t, J=7.3 Hz, 1H), 7.11 (d, J=7.6 Hz, 2H).

Aufarbeitung

  1. temperaturethe mixture was warmed up to room temperature
  2. stirringstirred for 30 minutes
  3. customThe layers were separated
  4. extractionThe aqueous layer was extracted twice with ethyl acetate
  5. extractionthe organic combined extract
  6. washwas washed with water, brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-e62fb9551e244d029c84549865eab78c
Quelldatensatz
uspto-grants-2007_03
Patentnummer
US07196108B2

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