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Nitric Acid → 4-Hydroxy-3-nitro-2(1H)-quinolinone

HRID 1450687
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인쇄 미리보기

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HRID 1450687 반응식
[N+:1]([O-:4])(O)=[O:2].[OH:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[NH:9][C:8](=[O:16])[CH:7]=1.O>C(O)(=O)C>[OH:5][C:6]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[NH:9][C:8](=[O:16])[C:7]=1[N+:1]([O-:4])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 962WaterHCID 546808712,4-Dihydroxyquinoline

생성물 1

HCID 546801624-Hydroxy-3-nitro-2(1H)-quinolinone수율 98%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
40 °C

실험 절차

Fuming nitric acid (262 mL) was added at about 20° C. to a suspension of 4-hydroxy-2(l H)-quinolinone (1.0 Kg) in acetic acid (7.57 L). The mixture was heated at 40° C. for 2.5 h. The resulting solution was cooled to about 20° C. and poured into 8 L of water. The resulting mixture was stirred for 20 rain, filtered, washed with water until the filtrate was neutral, and dried. The product 4-hydroxy-3-nitro-2(I H)-quinolinone was isolated in 98% yield and showed only one spot upon analysis by thin layer chromatography (silica gel, 20:80 (V/V) chloroform in methanol).

후처리

  1. temperatureThe resulting solution was cooled to about 20° C.
  2. filtrationfiltered
  3. washwashed with water until the filtrate
  4. customdried

출처 및 근거

ORD 기록
ord-072e97b0dde94b7490209af410026024
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05602256

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