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Diisopropyl Ether → 2,4-Di-tert-butyl-6-(prop-2-en-1-yl)phenol

HRID 1030449
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HRID 1030449 반응식
[C:1]([C:5]1[CH:10]=[C:9]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:8]=[CH:7][C:6]=1[O:15]CC=C)([CH3:4])([CH3:3])[CH3:2].[CH:19](OC(C)C)([CH3:21])[CH3:20]>>[CH2:21]([C:7]1[CH:8]=[C:9]([C:11]([CH3:12])([CH3:13])[CH3:14])[CH:10]=[C:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[C:6]=1[OH:15])[CH:19]=[CH2:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7914Diisopropyl EtherHCID 50888872HCID 50888872, 화합물

생성물 1

HCID 151106652,4-Di-tert-butyl-6-(prop-2-en-1-yl)phenol

실험 절차

10 g of 2,4-di-tert-butylallyloxybenzene are heated under nitrogen to 245° C. for 45 minutes. The yellow crude oil is taken up in diisopropyl ether. The ether phase is washed with 3 % sodium hydroxide and then with water. After drying and evaporation of the solvent, the oil obtained (7.6 g) is chromatographed on silica gel 60 (eluent: 80/20 heptane/CH2Cl2). A pale-yellow oil of 2-allyl-4,6-di-tert-butylphenol is obtained (5.4 g, yield =54 %).

후처리

  1. washThe ether phase is washed with 3 % sodium hydroxide
  2. customAfter drying
  3. customevaporation of the solvent
  4. customthe oil obtained (7.6 g)
  5. customis chromatographed on silica gel 60 (eluent: 80/20 heptane/CH2Cl2)
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출처 및 근거

ORD 기록
ord-d6fe5a38dc184a6690aa0d092ba36b39
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05106611

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