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Water → 3-Fluoro-4-(phenyl sulfonyl)benzeneamine

HRID 865759
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HRID 865759 반응식
[F:1][C:2]1[CH:3]=[C:4]([N+:15]([O-])=O)[CH:5]=[CH:6][C:7]=1[S:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[Mn]([O-])(=O)(=O)=[O:19].[K+].S([O-])([O-])=O.[Na+].[Na+].[OH2:30]>C(O)(=O)C>[F:1][C:2]1[CH:3]=[C:4]([NH2:15])[CH:5]=[CH:6][C:7]=1[S:8]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:19])=[O:30]
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참가 물질

6

반응물 4

HCID 962Water2회HCID 24437Sodium SulfiteHCID 516875Potassium PermanganateHCID 149263253-Fluoro-4-(phenylthio)nitrobenzene

생성물 1

HCID 107532343-Fluoro-4-(phenyl sulfonyl)benzeneamine수율 75%

시약·촉매·용매 1

HCID 176
Acetic Acid
용매

실험 절차

To a stirred solution of 3-fluoro-4-(phenylthio)nitrobenzene (5.65 g, 22.7 mmol) in glacial acetic acid (200 mL) was added potassium permanganate (4.30 g, 27.2 mmol) in distilled water (75 mL). The dark brown mixture was stirred at room temperature for 1 hour, then treated with solid sodium sulfite until the solution clarified. The mixture was diluted with water and filtered to yield an off-white solid. Recrystallization from absolute ethanol yielded the title sulfone (4.80 g, 75%) as an off-white solid; mp 124°-125° C. 1H-NMR (300 MHz, DMSO-d6): 7.68-7.73 (m, 2H, aromatic) 7.79-7.84 (m, 1H, aromatic) 8.00 (d, 2H, J=8.2 Hz, aromatic) 8.28-8.38 (m, 3H, aromatic). MS (CI, CH4): 282 (M+1).

후처리

  1. filtrationfiltered
  2. customto yield an off-white solid
  3. customRecrystallization from absolute ethanol

출처 및 근거

ORD 기록
ord-6c8b3f09ae10464484a464426d6283a4
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05567735

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