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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Nitric Acid → 5-Chloro-2-nitropyridin-3-ol

HRID 1624069
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HRID 1624069 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[N:6][CH:7]=1.[N+:9]([O-])([OH:11])=[O:10]>S(=O)(=O)(O)O>[Cl:1][C:2]1[CH:3]=[C:4]([OH:8])[C:5]([N+:9]([O-:11])=[O:10])=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 5823053-Hydroxy-5-chloropyridine

생성물 1

HCID 187656985-Chloro-2-nitropyridin-3-ol

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

With ice cooling, 30 g of 5-chloropyridin-3-ol (232 mmol, 1 equivalent) were dissolved in 228 ml of concentrated sulphuric acid, and, at 0° C., 24 ml of concentrated nitric acid were added slowly. The reaction was warmed to RT and stirred overnight. The mixture was stirred into an ice/water mixture and stirred for another 30 min. The solid was filtered off, washed with cold water and air-dried. This gave 33 g (82% of theory) of the title compound, which were used without further purification for the next reaction.

후처리

  1. stirringstirred for another 30 min
  2. filtrationThe solid was filtered off
  3. washwashed with cold water
  4. customair-dried
  5. customThis gave 33 g (82% of theory) of the title compound, which were used without further purification for the next reaction

출처 및 근거

ORD 기록
ord-de83379566284ea79db601c35568a006
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08778964B2

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