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Acetic Anhydride → HCID 15580724, 화합물

HRID 543812
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HRID 543812 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:12][CH:11]([CH3:13])[C:10]([NH:14][CH:15]=[O:16])=[N:9]2)=[CH:4][CH:3]=1.[C:17](OC(=O)C)(=O)C>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:12][CH:11]([CH3:13])[C:10]([NH:14][C:15](=[O:16])[CH3:17])=[N:9]2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 15580714HCID 15580714, 화합물

생성물 1

HCID 15580724HCID 15580724, 화합물

실험 절차

A 9.0 g. amount of 3-amino-1-(p-chlorophenyl)-4-methyl-2-pyrazoline (prepared as described in Example 23) is dissolved in 54.0 ml. of acetic anhydride. The warm solution is allowed to stand for 16 hours at room temperature with some solid separation. The solid is collected by filtration and is dissolved in methanol. Then 1 N potassium hydroxide in methanol is added to make basic. After 15 minutes at room temperature, the solvent is removed in vacuo and water is added to separate a solid. The solid is collected and recrystallized from dichloromethane-hexane to give 6.5 g. of the desired product as white crystals, m.p. 172°-173° C.

후처리

  1. customto stand for 16 hours at room temperature with some solid separation
  2. filtrationThe solid is collected by filtration
  3. dissolutionis dissolved in methanol
  4. addition
Then 1 N potassium hydroxide in methanol is added
  • customthe solvent is removed in vacuo and water
  • additionis added
  • customto separate a solid
  • customThe solid is collected
  • customrecrystallized from dichloromethane-hexane
  • customto give 6.5 g
  • 출처 및 근거

    ORD 기록
    ord-aae2abd47c6747e395b54bf9e68b78d9
    출처 데이터셋
    uspto-grants-1984_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04447442

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