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Dichloromethane → HCID 54468234, 화합물

HRID 234872
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인쇄 미리보기

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HRID 234872 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][CH2:10][O:11][N:12]2C(=O)C3=CC=CC=C3C2=O)=[CH:4][CH:3]=1.ClCCl>C(CN)O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[CH:9][CH2:10][O:11][NH2:12])=[CH:6][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6344DichloromethaneHCID 54486942HCID 54486942, 화합물

생성물 1

HCID 54468234HCID 54468234, 화합물수율 95.3%

시약·촉매·용매 1

HCID 700Ethanolamine용매

반응 조건

온도
30 °C

실험 절차

33.4 g (0.093 mol) of N-[3-(4-bromophenyl)-prop-2-enyloxy]phthalimide were introduced a little at a time in 50 ml of ethanolamine; the temperature increased to 30° C. during this procedure. Stirring was carried out for two hours at 60° C., after which the mixture was allowed to cool and 200 ml of dichloromethane were added. Extraction was effected by shaking with ice water. The organic phase was dried and evaporated down and the residue was crystallized from petroleum ether. Yield: 95.3%; m.p.: 35°-38° C.

후처리

  1. temperatureto cool
  2. extractionExtraction
  3. stirringby shaking with ice water
  4. customThe organic phase was dried
  5. customevaporated down
  6. customthe residue was crystallized from petroleum ether

출처 및 근거

ORD 기록
ord-2b71b1237e1e4811937a3e7c1dbae9c5
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05597776

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