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4-Chloro-2-nitroaniline → N-(4-chloro-2-nitrophenyl)acetamide

HRID 653047
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인쇄 미리보기

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HRID 653047 반응식
C(O[C:5](=[O:7])[CH3:6])(=O)C.[Cl:8][C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[C:11]([N+:16]([O-:18])=[O:17])[CH:10]=1>S(=O)(=O)(O)O.O>[C:5]([NH:13][C:12]1[CH:14]=[CH:15][C:9]([Cl:8])=[CH:10][C:11]=1[N+:16]([O-:18])=[O:17])(=[O:7])[CH3:6]
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참가 물질

5

반응물 2

HCID 69794-Chloro-2-nitroanilineHCID 7918Acetic Anhydride

생성물 1

HCID 2788431N-(4-chloro-2-nitrophenyl)acetamide

시약·촉매·용매 2

HCID 1118Sulfuric Acid촉매HCID 962Water용매

반응 조건

온도
50 °C

실험 절차

To a mixture of 50 ml of acetic anhydride and two drops of sulfuric acid was added 34.5 grams of 4-chloro-2-nitroaniline in several portions. At the end of addition, the solution was heated at 50° C. for one hour and then allowed to cool. 300 ml of cold water was added to the solution to induce precipitation of crystals, which were removed by filtration and washed with water. There were obtained the crystals of 2-acetylamino-5-chloronitrobenzene in a yield of 41.8 grams.

후처리

  1. additionAt the end of addition
  2. temperatureto cool
  3. customprecipitation of crystals, which
  4. customwere removed by filtration
  5. washwashed with water

출처 및 근거

ORD 기록
ord-4dec328e5bcd40e98eb823388ebab255
출처 데이터셋
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04675277

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