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Sodium Bicarbonate → 2-Hydroxymethyl-2,4,6,7-tetramethyldihydrobenzofuran

HRID 1987773
ノート
印刷プレビュー

反応式

HRID 1987773 の反応式
[CH3:1][C:2](=[CH2:14])[CH2:3][C:4]1[C:9]([CH3:10])=[CH:8][C:7]([CH3:11])=[C:6]([CH3:12])[C:5]=1[OH:13].C(=O)([O-])[OH:16].[Na+]>C(Cl)Cl>[OH:16][CH2:14][C:2]1([CH3:1])[CH2:3][CH:4]2[CH:9]([CH3:10])[CH:8]=[C:7]([CH3:11])[C:6]([CH3:12])=[C:5]2[O:13]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 516892Sodium BicarbonateHCID 10655310Phenol, 2,3,5-trimethyl-6-(2-methyl-2-propenyl)-

生成物 1

HCID 688473332-Hydroxymethyl-2,4,6,7-tetramethyldihydrobenzofuran

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

31.86 g of 2-(2-methyl-2-propenyl)-3,5,6-trimethylphenol was dissolved in 600 ml of methylene chloride and 47.5 g of methchloroperbenzoic acid was gradually charged while maintaining at 0° C. After stirring at 0° C. for 2 hours, the solution was poured into an aqueous sodium hydrogen carbonate. The organic layer was extracted with chloroform, washed with an aqueous saturated sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate and, after the solvent was distilled off, the residue was purified by silica gel column chromatography (chloroform) to obtain 17 g of the objective product.

後処理

  1. extractionThe organic layer was extracted with chloroform
  2. washwashed with an aqueous saturated sodium hydrogen carbonate solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationafter the solvent was distilled off
  5. customthe residue was purified by silica gel column chromatography (chloroform)

出典と根拠

ORDレコード
ord-2f833f6ed1534ae9b596ad94690411f9
出典データセット
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07553837B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート