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Sulfuric Acid → 2,2,4,4,7-Pentamethyl-chroman

HRID 373415
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HRID 373415 반응식
[CH3:1][C:2]([C:9]1[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][C:10]=1[OH:16])([CH3:8])[CH2:3][C:4]([CH3:7])(O)[CH3:5].S(=O)(=O)(O)O>>[CH3:7][C:4]1([CH3:5])[CH2:3][C:2]([CH3:1])([CH3:8])[C:9]2[C:10](=[CH:11][C:12]([CH3:15])=[CH:13][CH:14]=2)[O:16]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 1118Sulfuric AcidHCID 156611222-(1,1,3-Trimethyl-3-hydroxybutyl) 5-methyl-phenol2회

생성물 1

HCID 156611242,2,4,4,7-Pentamethyl-chroman

실험 절차

To 2.16 g (11.7 mmol) of 2-(1,1,3-trimethyl-3-hydroxybutyl) 5-methyl-phenol (Compound 45) was added under nitrogen 50 ml of 20% aqueous sulfuric acid. The reaction mixture was heated at reflux for 13 h and then cooled. The organic layer was separated and the aqueous layer was extracted with ether. The organic extracts were combined and washed successively with water, saturated NaHCO3 solution, water again and saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo to give the title compound as a yellow oil. PMR (CDCl3): & 1.32 (6H, s), 1.34 (6H, s), 1.81 (2H, s), 2.26 (3H, s), 6.63 (1H, s), 6.72 (1H, d, J~7.9 Hz), 7.15 (1H, d, J~7.9 Hz).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 13 h
  • temperaturecooled
  • customThe organic layer was separated
  • extractionthe aqueous layer was extracted with ether
  • washwashed successively with water, saturated NaHCO3 solution, water again
  • dry with materialsaturated NaCl solution and then dried (MgSO4)
  • customThe solvent was removed in vacuo
  • 출처 및 근거

    ORD 기록
    ord-ccc5fdc18b21424eae9c540743e1678d
    출처 데이터셋
    uspto-grants-1992_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05162546

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