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Sulfuric Acid → HCID 18506076, 화합물

HRID 1357371
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반응식

HRID 1357371 반응식
[NH2:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[O:4][C:5]1[CH:6]=[C:7](C#N)[C:8](=[CH:11][CH:12]=1)[C:9]#[N:10].S(=O)(=O)(O)[OH:20].[C:24](=[O:27])([O-])O.[Na+]>O>[NH2:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[O:4][C:5]1[CH:6]=[C:7]2[C:8](=[CH:11][CH:12]=1)[C:9](=[O:20])[NH:10][C:24]2=[O:27]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 516892Sodium BicarbonateHCID 18506202HCID 18506202, 화합물

생성물 1

HCID 18506076HCID 18506076, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

4-(2-Aminophenoxy)phthalonitrile (1.55 g, 6.6 mmol) was stirred with conc. sulphuric acid (9 ml) at room temperature for 15 hours. The mixture was purred into crushed ice and the pH was adjusted to 10 with diluted sodium hydrogencarbonate in water. The mixture was left for the weekend at room temperature. The resulting precipitate was filtered off and washed twice with water (2×50 ml). The crystals were dried to give yellow crystals of 5-(2-aminophenoxy)isoindole-1,3dione) (yield: 1.41 g (84%)). Mp: 211.6-211.9° C.

후처리

  1. custominto crushed ice
  2. waitThe mixture was left for the weekend at room temperature
  3. filtrationThe resulting precipitate was filtered off
  4. washwashed twice with water (2×50 ml)
  5. customThe crystals were dried

출처 및 근거

ORD 기록
ord-73e5f308f7f34d218d270ffea72d3bc5
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06590118B1

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