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Nitric Acid → 2-(4-Bromo-3-nitro-phenyl)-3-(trifluoromethyl)-pyridine

HRID 1791219
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반응식

HRID 1791219 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([C:14]([F:17])([F:16])[F:15])=[CH:12][CH:11]=[CH:10][N:9]=2)=[CH:4][CH:3]=1.[N+:18]([O-])([OH:20])=[O:19]>OS(O)(=O)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:13]([C:14]([F:17])([F:15])[F:16])=[CH:12][CH:11]=[CH:10][N:9]=2)=[CH:6][C:7]=1[N+:18]([O-:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 220302682-(4-Bromophenyl)-3-(trifluoromethyl)-pyridine

생성물 1

HCID 220301962-(4-Bromo-3-nitro-phenyl)-3-(trifluoromethyl)-pyridine

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a solution of 2-(4-bromophenyl)-3-(trifluoromethyl)-pyridine (0.93 mmol) in H2SO4 (4 mL) cautiously add fuming HNO3 (2 ml). Stir the mixture 30 minutes at room temperature. Pour the mixture onto ice-water (20 mL) and collect the precipitate. Dissolve the precipitate in EtOAc and neutralize with saturated NaHCO3, dry over Na2SO4, concentrate under vacuum to obtain 2-(4-bromo-3-nitro-phenyl)-3-(trifluoromethyl)-pyridine.

후처리

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  1. additionPour the mixture onto ice-water (20 mL)
  2. customcollect the precipitate
  3. dissolutionDissolve the precipitate in EtOAc
  4. dry with materialdry over Na2SO4
  5. concentrationconcentrate under vacuum

출처 및 근거

ORD 기록
ord-4e8cb0995cf849da806203796dbca3c7
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074799B2

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