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Hydrogen Peroxide → 2,4-Dibenzyloxyphenol

HRID 322862
ノート
印刷プレビュー

反応式

HRID 322862 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 784Hydrogen PeroxideHCID 24437Sodium SulfiteHCID 10870855Dibenzyloxybenzaldehyde

生成物 1

HCID 106383482,4-Dibenzyloxyphenol収率 41.6%

試薬・触媒・溶媒 2

HCID 1118Sulfuric Acid触媒HCID 887Methanol溶媒

実験手順

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%].

後処理

  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

出典と根拠

ORDレコード
ord-fe40040671c04339b28dd52e0ac87024
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06211234B1

反応ノート

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