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Methyl iodide → HCID 70596703, 화합물

HRID 1395655
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HRID 1395655 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:16]1[S:17][CH:18]=[CH:19][CH:20]=1)=[C:7]1[CH2:15][N:14]2[CH:9]([CH2:10][CH2:11][CH2:12][CH2:13]2)[CH2:8]1.[CH3:21][I:22]>CC(C)=O>[CH3:21][I:22].[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([C:16]1[S:17][CH:18]=[CH:19][CH:20]=1)=[C:7]1[CH2:15][N:14]2[CH:9]([CH2:10][CH2:11][CH2:12][CH2:13]2)[CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 70594925HCID 70594925, 화합물

생성물 1

HCID 70596703HCID 70596703, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

In 5 ml. of acetone was dissolved 0.37 g. of 2-(dithien-2-ylmethylene)indolizidine. To the resulting solution was added 1.0 ml. of methyl iodide. The mixture was stirred at room temperature for 3 hrs. The formed crystals were taken out by filtration. By recrystallization from isopropanol, 0.15 g. of colorless or light brown prisms having a melting point of 222° to 225° C. were obtained.

후처리

  1. additionTo the resulting solution was added 1.0 ml
  2. filtration
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
The formed crystals were taken out by filtration
  • customBy recrystallization from isopropanol, 0.15 g
  • customwere obtained
  • 출처 및 근거

    ORD 기록
    ord-fd7d3545c04e493c95d8d22fd92821fa
    출처 데이터셋
    uspto-grants-1980_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04205074

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