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

HRID 606355

Reaktionsgleichung

Reaktionsgleichung von HRID 606355
[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-998a6b0a68ca4010ae19d6905b538376
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07915295B2

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