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Nitric Acid → 2-(4-Chloro-6-fluoro-3-hydroxy-2-nitrophenyl)-5-trifluoromethylpyridazin-3-one

HRID 1271767
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반응식

HRID 1271767 반응식
[N+:1]([O-:4])(O)=[O:2].[Cl:5][C:6]1[C:11]([OH:12])=[CH:10][C:9]([N:13]2[C:18](=[O:19])[CH:17]=[C:16]([C:20]([F:23])([F:22])[F:21])[CH:15]=[N:14]2)=[C:8]([F:24])[CH:7]=1>>[Cl:5][C:6]1[CH:7]=[C:8]([F:24])[C:9]([N:13]2[C:18](=[O:19])[CH:17]=[C:16]([C:20]([F:21])([F:22])[F:23])[CH:15]=[N:14]2)=[C:10]([N+:1]([O-:4])=[O:2])[C:11]=1[OH:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 944Nitric AcidHCID 114040782-(4-Chloro-2-fluoro-5-hydroxyphenyl)-5-trifluoromethylpyridazin-3-one

생성물 1

HCID 186156602-(4-Chloro-6-fluoro-3-hydroxy-2-nitrophenyl)-5-trifluoromethylpyridazin-3-one

실험 절차

Nitric acid (70%, 12 ml) was added to the ice-cooled 2-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-trifluoromethylpyridazin-3-one (1.25 g) and stirred at room temperature for 30 minutes. Crushed ice was added. The precipitate was collected by filtration and washed with water to give 1.20 g of the desired product, m.p. 146-8° C.

후처리

  1. additionCrushed ice was added
  2. filtrationThe precipitate was collected by filtration
  3. washwashed with water

출처 및 근거

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
ORD 기록
ord-c6ceb8937fd9419e8c1ded7cb99e546d
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE039590E1

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