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Nitric Acid → HCID 178526872, 화합물

HRID 432698
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HRID 432698 반응식
[N:1]1[N:5]2[C:6]3[C:11]([C:12]([OH:14])=[CH:13][C:4]2=[N:3][N:2]=1)=[CH:10][CH:9]=[CH:8][CH:7]=3.[N+:15]([O-])([OH:17])=[O:16]>C(O)(=O)C>[N+:15]([C:13]1[C:4]2[N:5]([N:1]=[N:2][N:3]=2)[C:6]2[C:11]([C:12]=1[OH:14])=[CH:10][CH:9]=[CH:8][CH:7]=2)([O-:17])=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 178515414HCID 178515414, 화합물

생성물 1

HCID 178526872HCID 178526872, 화합물수율 76.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
52.5 °C

실험 절차

Tetrazolo[1,5-a]quinolin-5-ol (63.25 g, 0.34 mol) was added to glacial acetic acid (630 ml) to form a thick off white suspension. The mixture was vigorously stirred while nitric acid (23.6 ml, 0.37 mol, 70% solution) was slowly added. The reaction was then heated from 25 to 80° C. over a period of 15 minutes. A yellow precipitate formed and the reaction was maintained at 80° C. for 5 minutes. The mixture was slowly cooled to 0° C. The solid was collected by filtration and then dried in vacuo to yield 60.0 g of 4-nitro-tetrazolo[1,5-a]quinolin-5-ol as a yellow solid.

후처리

  1. customto form a thick off white suspension
  2. additionwas slowly added
  3. customA yellow precipitate formed
  4. temperaturethe reaction was maintained at 80° C. for 5 minutes
  5. temperatureThe mixture was slowly cooled to 0° C
  6. filtrationThe solid was collected by filtration
  7. customdried in vacuo

출처 및 근거

ORD 기록
ord-b2e17b2db7914aa7b4785cf27fdefc79
출처 데이터셋
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06664260B2

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