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Sulfuric Acid → 2-(Hydroxymethyl)-4-(trifluoromethyl)phenol

HRID 1081876
ノート
印刷プレビュー

反応式

HRID 1081876 の反応式
COC[O:4][C:5]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:6]=1[CH2:7][OH:8].OS(O)(=O)=O>CO>[OH:8][CH2:7][C:6]1[CH:9]=[C:10]([C:13]([F:15])([F:16])[F:14])[CH:11]=[CH:12][C:5]=1[OH:4]
参加物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 1118Sulfuric AcidHCID 543883822-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol

生成物 1

HCID 233631292-(Hydroxymethyl)-4-(trifluoromethyl)phenol収率 98%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To the solution of 2-methoxymethoxy-5-(trifluoromethyl)benzyl alcohol (3.15 g) from Example 60 in methanol (20 ml) was added 10% H2SO4 (5 ml) for reflux under heating for 1 hour. The solvent was removed under reduced pressure. To the residue was added water, the aqueous layer was extracted with ether. The ether layer was washed with water and saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, to give the title compound (2.5 g; 98%).

後処理

  1. temperaturefor reflux
  2. temperatureunder heating for 1 hour
  3. customThe solvent was removed under reduced pressure
  4. additionTo the residue was added water
  5. extractionthe aqueous layer was extracted with ether
  6. washThe ether layer was washed with water and saturated sodium chloride solution
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-d66bc06660dd4cf3b374e6e6b8b1da33
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05587392

反応ノート

読み込み中…

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