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

HRID 2110978

반응식

HRID 2110978 반응식
[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

참가 물질

4

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-43481a2c88764119b07d1370a430297b
출처 데이터셋
uspto-grants-2009_04
특허 번호
US07517992B2

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