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Nitric Acid → HCID 22030083, 화합물

HRID 1791264
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HRID 1791264 반응식
[F:1][C:2]([F:17])([F:16])[C:3]1[C:4]([C:9]2[CH:14]=[CH:13][C:12](=[O:15])[NH:11][CH:10]=2)=[N:5][CH:6]=[CH:7][CH:8]=1.[N+:18]([O-])([OH:20])=[O:19]>S(=O)(=O)(O)O>[N+:18]([C:13]1[C:12](=[O:15])[NH:11][CH:10]=[C:9]([C:4]2[C:3]([C:2]([F:16])([F:1])[F:17])=[CH:8][CH:7]=[CH:6][N:5]=2)[CH:14]=1)([O-:20])=[O:19]
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참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 22030009HCID 22030009, 화합물

생성물 1

HCID 22030083HCID 22030083, 화합물수율 92%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

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온도
70 °C

실험 절차

To a solution of 3-trifluoromethyl-1′H-[2,3′]bipyridinyl-6′-one (25 g, 0.1 mol) in concentrated sulfuric acid (100 mL) at 0° C., add dropwise a solution of fuming nitric acid (35 mL) and concentrated sulfuric acid (10 mL). Heat the reaction mixture to 70° C. for 1 hour, cool and pour onto ice (500 mL). Filter the mixture and treat the filtrate with 10 M sodium hydroxide until the solution is at pH 4-5. Collect the precipitate by filtration and air dry to give the title compound (26.2 g, 92%) as a white solid.

후처리

  1. temperaturecool
  2. additionpour onto ice (500 mL)
  3. filtrationFilter the mixture
  4. additiontreat the filtrate with 10 M sodium hydroxide until the solution
  5. customCollect the precipitate
  6. filtrationby filtration and air
  7. customdry

출처 및 근거

ORD 기록
ord-05492f6a96b7429db4e0da67867767ff
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074799B2

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