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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Peroxide → 5,6-dichloropyridine-2-carboxylic acid-N-oxide

HRID 1837436
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HRID 1837436 반응식
OO.[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([C:11]([OH:13])=[O:12])=[N:8][C:9]=1[Cl:10].[OH:14]S([O-])=O.[Na+]>FC(F)(F)C(O)=O>[Cl:3][C:4]1[C:9]([Cl:10])=[N+:8]([O-:14])[C:7]([C:11]([OH:13])=[O:12])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 784Hydrogen PeroxideHCID 132780162-Pyridinecarboxylic acid, 5,6-dichloro-HCID 23665763Sodium Bisulfite

생성물 1

HCID 129936895,6-dichloropyridine-2-carboxylic acid-N-oxide

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

50% Hydrogen peroxide (38 g, 0.35 mol) was carefully added to a mechanically stirred mixture of trifluoroacetic acid (350 mL) and 5,6-dichloropyridine-2-carboxylic acid (56.4 g, 0.29 mol) at 79° C. After one hour, the reaction mixture was poured into 1 L of saturated aqueous NaHSO3, stirring vigorously and cooling in an ice bath. The precipitate was collected and dried to provide 5,6-dichloropyridine-2-carboxylic acid-N-oxide (62.9 g, 0.30 mol), mp 160° C.

후처리

  1. temperaturecooling in an ice bath
  2. customThe precipitate was collected
  3. customdried

출처 및 근거

ORD 기록
ord-13e6f9fb0c974244bd1fff3fa373763a
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06784137B2

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