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

HRID 1081876
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HRID 1081876 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 543883822-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol

생성물 1

HCID 233631292-(Hydroxymethyl)-4-(trifluoromethyl)phenol수율 98%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-d66bc06660dd4cf3b374e6e6b8b1da33
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05587392

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