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Acetic Anhydride → HCID 21406318, 화합물

HRID 972207
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인쇄 미리보기

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HRID 972207 반응식
[Br:1][C:2]1[C:3]([OH:17])=[C:4]([C:10]2[CH:11]=[CH:12][C:13](=[O:16])[NH:14][N:15]=2)[CH:5]=[C:6]([Br:9])[C:7]=1[CH3:8].[C:18](OC(=O)C)(=[O:20])[CH3:19]>C1C=CC=CC=1>[C:18]([O:17][C:3]1[C:2]([Br:1])=[C:7]([CH3:8])[C:6]([Br:9])=[CH:5][C:4]=1[C:10]1[CH:11]=[CH:12][C:13](=[O:16])[NH:14][N:15]=1)(=[O:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 13627389662902-45-8

생성물 1

HCID 21406318HCID 21406318, 화합물수율 71.5%

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A mixture of 1.0 g. of 6-(3,5-dibromo-2-hydroxy-4-methylphenyl)-3-(2H)pyridazinone and 2 ml. of acetic anhydride in 10 ml. of benzene was heated under reflux for 3 hours. After cooling, the so separated crystalline substance was recovered by filtration and dried to give 0.8 g. of the desired product as yellow needles of m.p. 220° C. (Yield 71.5%).

후처리

  1. additionA mixture of 1.0 g
  2. temperatureunder reflux for 3 hours
  3. temperatureAfter cooling
  4. filtrationthe so separated crystalline substance was recovered by filtration
  5. customdried
  6. customto give 0.8 g

출처 및 근거

ORD 기록
ord-6b325ba319214b5088613f095aa73d09
출처 데이터셋
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04052395

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