gamma-Propanol → 4-(3-Hyd-roxypropyl)-2-t-butylphenol

HRID 64952

반응식

HRID 64952 반응식
[C:1]([C:5]1[CH:6]=[C:7]([CH2:16][CH2:17][CH2:18][OH:19])[CH:8]=[C:9](C(C)(C)C)[C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2]>FC(F)(F)C(O)=O>[C:1]([C:5]1[CH:6]=[C:7]([CH2:16][CH2:17][CH2:18][OH:19])[CH:8]=[CH:9][C:10]=1[OH:11])([CH3:4])([CH3:2])[CH3:3]

참가 물질

3

반응 조건

온도
40 °C

실험 절차

3-(3',5'-Di-tert-butyl-4'-hydroxyphenyl)-1-propanol (100 g, 0.38 mol) was dissolved in 500 ml of trifluoracetic acid. The solution was stirred at 40° C. for six hours, then poured into an ice-water mixture. The mixture was extracted with methylene chloride. The methylene chloride layer was washed with aqueous sodium carbonate and evaporated. A solution of sodium hydroxide (25 g) in 400 ml of methanol was added to the residue. The mixture was stirred at room temperature for 30 minutes, neutralized with 1N hydrochloric acid and extracted with methylene chloride. The methylene chloride layer was washed with aqueous sodium carbonate and water, dried with anhydrous sodium sulfate, and evaporated. The residue was vacuum distilled to give 51 g (64%) of the product.

후처리

  1. extractionThe mixture was extracted with methylene chloride
  2. washThe methylene chloride layer was washed with aqueous sodium carbonate
  3. customevaporated
  4. additionA solution of sodium hydroxide (25 g) in 400 ml of methanol was added to the residue
  5. stirringThe mixture was stirred at room temperature for 30 minutes
  6. extractionextracted with methylene chloride
  7. washThe methylene chloride layer was washed with aqueous sodium carbonate and water
  8. dry with materialdried with anhydrous sodium sulfate
  9. customevaporated
  10. distillationdistilled

출처 및 근거

ORD 기록
ord-9cc013f1ccc74a27a6d955c9407b5717
출처 데이터셋
uspto-grants-1986_09
특허 번호
US04611061

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