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Sodium Dithionite → 2-{[2-Amino-6-(trifluoromethyl)phenyl]amino}ethanol

HRID 1991200
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HRID 1991200 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:13])([F:12])[F:11])[C:5]=1[NH:14][CH2:15][CH2:16][OH:17])([O-])=O.S(S([O-])=O)([O-])=O.[Na+].[Na+]>CO.O>[NH2:1][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:12])([F:13])[F:11])[C:5]=1[NH:14][CH2:15][CH2:16][OH:17]
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참가 물질

5

반응물 2

HCID 24489Sodium DithioniteHCID 113571292-([2-Nitro-6-(trifluoromethyl)phenyl]amino}ethanol

생성물 1

HCID 111953562-{[2-Amino-6-(trifluoromethyl)phenyl]amino}ethanol수율 89.9%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매2회

반응 조건

온도
60 °C

실험 절차

To a solution of 2-{[2-nitro-6-(trifluoromethyl)phenyl]amino}ethanol (0.72 g, 2.88 mmol) in methanol (30 mL) a suspension of 85% sodium hydrosulfite (2.0 g, 9.8 mmol) in water (6 mL) was added. Additional water (4 mL) was added, and the mixture was heated at 60° C. for 15 min. The reaction mixture was cooled and concentrated in vacuo. The residue was extracted with ethyl acetate, and the organic phase was dried over magnesium sulfate. The solvent was removed in vacuo affording 0.57 g of 2-{[2-amino-6-(trifluoromethyl)phenyl]amino}ethanol: MS (ES) m/z 219 [M−H].

후처리

  1. additionwas added
  2. temperatureThe reaction mixture was cooled
  3. concentrationconcentrated in vacuo
  4. extractionThe residue was extracted with ethyl acetate
  5. dry with materialthe organic phase was dried over magnesium sulfate
  6. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-cea36f64a7de4acea5ec0ce77d5b489a
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07645784B2

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