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p-Toluenesulfonic acid → 2,2,4,5-Tetramethyl-4-hexen-3-one

HRID 440637
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HRID 440637 반응식
[CH3:1][C:2]([CH3:11])([C:4](=[O:10])[CH:5]([CH3:9])[C:6]([CH3:8])=[CH2:7])[CH3:3].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[CH3:3][C:2]([CH3:11])([C:4](=[O:10])[C:5]([CH3:9])=[C:6]([CH3:8])[CH3:7])[CH3:1]
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참가 물질

4

반응물 2

HCID 6101p-Toluenesulfonic acidHCID 118159642,2,4,5-Tetramethyl-5-hexen-3-one

생성물 1

HCID 112521302,2,4,5-Tetramethyl-4-hexen-3-one

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

30.8 g (0.2 mole) of 2,2,4,5-tetramethyl-5-hexen-3-one were heated to 100° in 100 ml of toluene in the presence of 3.08 g of p-toluenesulfonic acid. After 24 h, the mixture was cooled down and extracted with ether. After neutralizing with an aqueous solution saturated with NaHCO3, the organic phase was washed with water, then with a solution saturated with NaCl, and dried with Na2SO4. Evaporation and distillation of the residue, followed by fractional distillation, provided a fraction having B.p. 60°/1.06×103Pa NMR(1H, 360MHz): 1.18(s, 9H); 1.57(s, 3H); 1.66(s, 3H); 1.77(s, 3H) δppm MS:m/z:154(3, M+), 97(100), 69(62), 41(65), 39(20).

후처리

  1. temperaturethe mixture was cooled down
  2. extractionextracted with ether
  3. washthe organic phase was washed with water
  4. dry with materialwith a solution saturated with NaCl, and dried with Na2SO4
  5. customEvaporation and distillation of the residue
  6. distillationfollowed by fractional distillation
  7. customprovided a fraction

출처 및 근거

ORD 기록
ord-fedafcc0e7064269a05f2f541a971f1c
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05521151

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