6-Methoxy-alpha-tetralone → 6-Methoxy-1,2,3,4-tetrahydronaphthalen-1-ol

HRID 2110978

Reaktionsgleichung

Reaktionsgleichung von HRID 2110978
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[C:9](=[O:13])[CH2:8][CH2:7][CH2:6]2.[BH4-].[Na+]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]([OH:13])[CH2:8][CH2:7][CH2:6]2

Komponenten

4

Versuchsvorschrift

6-Methoxytetralone (10 g, 0.057 mol) was mixed with 150 ml of dry ethanol and sodium borohydride (1.2 eq) was added by portions to the stirred mixture. The reaction mixture was left to stir at ambient temperature for 15 h. The reaction mixture was then concentrated by rotary evaporation, mixed with 100 ml of water and heated for 1 h at 45° C. The resulting mixture was extracted into diethyl ether (3×80 ml). Combined organic extract was dried over Na2SO4 and concentrated by rotary evaporation to give 10.39 g of yellow oil which was used in the next step without additional purification.

Aufarbeitung

  1. additionwas added by portions to the stirred mixture
  2. waitThe reaction mixture was left
  3. concentrationThe reaction mixture was then concentrated by rotary evaporation
  4. additionmixed with 100 ml of water
  5. temperatureheated for 1 h at 45° C
  6. extractionThe resulting mixture was extracted into diethyl ether (3×80 ml)
  7. extractionCombined organic extract
  8. dry with materialwas dried over Na2SO4
  9. concentrationconcentrated by rotary evaporation

Quellen und Nachweise

ORD-Eintrag
ord-43481a2c88764119b07d1370a430297b
Quelldatensatz
uspto-grants-2009_04
Patentnummer
US07517992B2

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