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Hydrogen Peroxide → 2,4-Dibenzyloxyphenol

HRID 322862
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HRID 322862 반응식
C([O:8][C:9]1[C:10]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[C:11]([CH:14]=[CH:15][CH:16]=1)C=O)C1C=CC=CC=1.OO.S([O-])([O-])=O.[Na+].[Na+]>S(=O)(=O)(O)O.CO>[CH2:18]([O:17][C:10]1[CH:11]=[C:14]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:15]=[CH:16][C:9]=1[OH:8])[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1
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참가 물질

6

반응물 3

HCID 784Hydrogen PeroxideHCID 24437Sodium SulfiteHCID 10870855Dibenzyloxybenzaldehyde

생성물 1

HCID 106383482,4-Dibenzyloxyphenol수율 41.6%

시약·촉매·용매 2

HCID 1118Sulfuric Acid촉매HCID 887Methanol용매

실험 절차

Concentrated sulphuric acid (2-3 drops) is added to a stirred solution of dibenzyloxybenzaldehyde (1.5 g) in methanol (50 mL), resulting in a thick precipitate. The mixture is stirred for 5 minutes then hydrogen peroxide (1 g; 27.5% in water) is added in one portion and stirring is continued for 2 hours. The resulting brown solution is treated with 10% aqueous sodium sulphite solution (10 mL) then evaporated to low bulk. The residue is treated with water (50 mL), the solid washed with water, dried and crystallised from cyclohexane, with charcoal treatment, to give 2,4-dibenzyloxyphenol (0.3 g) as a white powder, m.p. 82-83° C. [Elemental analysis:- C,78.2; H,5.79%. Calculated:- C,78.4; H,5.92%].

후처리

  1. customresulting in a thick precipitate
  2. stirringstirring
  3. waitis continued for 2 hours
  4. customthen evaporated to low bulk
  5. additionThe residue is treated with water (50 mL)
  6. washthe solid washed with water
  7. customdried
  8. customcrystallised from cyclohexane, with charcoal treatment

출처 및 근거

ORD 기록
ord-fe40040671c04339b28dd52e0ac87024
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06211234B1

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