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Water → 4-(Methylsulfonyl)-3-(trifluoromethyl)aniline

HRID 497239
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HRID 497239 반응식
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-])=O)=[CH:7][C:6]=1[C:14]([F:17])([F:16])[F:15])(=[O:4])=[O:3].[Cl-].[NH4+].O>C(O)C.[Fe]>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([NH2:11])=[CH:7][C:6]=1[C:14]([F:15])([F:16])[F:17])(=[O:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 206051531-(Methylsulphonyl)-4-nitro-2-(trifluoromethyl)benzene

생성물 1

HCID 223166824-(Methylsulfonyl)-3-(trifluoromethyl)aniline수율 76.2%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 702Ethanol용매

실험 절차

A mixture of 4-(methylsulfonyl)-3-(trifluoromethyl)nitrobenzene (1.55 g, 5.76 mmol), iron powder (1.61 g, 28.8 mmol), and ammonium chloride (0.03.1 g, 0.58 mmol) in ethanol (30 mL), and water (8 mL) was heated at reflux temperature for 1 hour. After cooling, insolubles were filtered off by Celite, and volatiles were removed by evaporation. The residue was redissolved in ethyl acetate (50 mL) and the whole washed with water and brine. After dried over MgSO4 and concentration in vacuo. The residue was washed with hexane to give the subtitle compound (1.05 g, 76.2%, yield).

후처리

  1. temperaturewas heated
  2. temperatureat reflux temperature for 1 hour
  3. temperatureAfter cooling
  4. filtrationinsolubles were filtered off by Celite, and volatiles
  5. customwere removed by evaporation
  6. dissolutionThe residue was redissolved in ethyl acetate (50 mL)
  7. washthe whole washed with water and brine
  8. dry with materialAfter dried over MgSO4 and concentration in vacuo
  9. washThe residue was washed with hexane

출처 및 근거

ORD 기록
ord-baa5ca339624476d9e3436f342e7e966
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06949536B2

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