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Nitric Acid → 3-Methylsulfonyl-4-trifluoromethoxynitrobenzene

HRID 1633939
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인쇄 미리보기

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HRID 1633939 반응식
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[O:11][C:12]([F:15])([F:14])[F:13])(=[O:4])=[O:3].[N+:16]([O-])([OH:18])=[O:17]>S(=O)(=O)(O)O>[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([N+:16]([O-:18])=[O:17])[CH:8]=[CH:7][C:6]=1[O:11][C:12]([F:13])([F:14])[F:15])(=[O:4])=[O:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 223110911-Methylsulfonyl-2-trifluoromethoxybenzene

생성물 1

HCID 223111663-Methylsulfonyl-4-trifluoromethoxynitrobenzene

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

반응 조건

온도
40 °C

실험 절차

1-Methylsulfonyl-2-trifluoromethoxybenzene (15.7 g, 65 mmol) was dissolved in concentrated sulfuric acid (27 mL) and the solution was heated to 40° C. Nitric acid (100%, 27 mL) was added dropwise over 45 minutes. The reaction mixture was allowed to stand overnight at 60° C., cooled, and then poured on crushed ice (300 mL). The precipitated product was isolated by filtration, washed with water (10×50 mL) and dried (MgSO4), affording 17.5 g of 3-methylsulfonyl-4-trifluoromethoxynitrobenzene.

후처리

  1. temperaturecooled
  2. additionpoured
  3. customThe precipitated product was isolated by filtration
  4. washwashed with water (10×50 mL)
  5. dry with materialdried (MgSO4)

출처 및 근거

ORD 기록
ord-923dbb4fd66a43339ad1ba2f9376f2fd
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06503949B1

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