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Acetic Acid → 3-Amino-5-(trifluoromethyl)phenol

HRID 446271
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HRID 446271 반응식
C[O:2][C:3]1[CH:4]=[C:5]([NH2:13])[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.Br.C(O)(=O)C>O>[NH2:13][C:5]1[CH:4]=[C:3]([OH:2])[CH:8]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:6]=1
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 260Hydrogen BromideHCID 6056715-(Trifluoromethyl)-m-anisidine

생성물 1

HCID 144012293-Amino-5-(trifluoromethyl)phenol수율 81%

시약·촉매·용매 1

HCID 962Water용매

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온도
140 °C

실험 절차

To a round bottom flask was added 3-methoxy-5-trifluoromethyl-phenylamine (1.0 g, 5.23 mmol), 10 mL HBr (49% aq.), and 8 mL glacial acetic acid. A reflux condenser was attached and the solution heated to 140° C. for 20 h. The reaction was then diluted with water and neutralized to ˜pH 7 by slow addition of saturated NaHCO2. The aqueous solution was then extracted into EtOAc twice. The organic layers were combined, washed once with brine, dried over Mg2SO4, filtered, and concentrated in vacuo to yield the title compound as a tan solid (750 mg). MS (M+H)+=178; Calc'd 177.12 for C7H6F3NO.

후처리

  1. customA reflux condenser was attached
  2. extractionThe aqueous solution was then extracted into EtOAc twice
  3. washwashed once with brine
  4. dry with materialdried over Mg2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0f766a72f2b84ad7848bb3beacd11583
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08476434B2

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