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2-Tolyl isocyanate → o-Tolyl Urea Styrene

HRID 1609682
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HRID 1609682 반응식
[NH2:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1.[C:10]1([CH3:19])[C:11]([N:16]=[C:17]=[O:18])=[CH:12][CH:13]=[CH:14][CH:15]=1>C(Cl)(Cl)Cl>[CH2:7]=[CH:6][C:5]1[CH:8]=[CH:9][CH:2]=[CH:3][CH:4]=1.[C:10]1([CH3:19])[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH:16][C:17]([NH2:1])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 691942-Tolyl isocyanateHCID 737004-Aminostyrene

생성물 1

HCID 19390271o-Tolyl Urea Styrene

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

1.00 g (8.40 mmol) of p-aminostyrene (99% Tokyo Kasei) was added to a 250 ml round bottom flask containing 10 ml of chloroform. After ten minutes of mixing, 1.12 g (8.41 mmol) of o-tolyl isocyanate (99% Aldrich) was added dropwise. Within seconds, a yellow precipitate formed. The precipitate was filtered to remove the reaction liquid, then washed with 20 ml of chloroform resulting in pale yellow powder (1.45 g, 68% crude yield, mp=193° C.).

후처리

  1. additionAfter ten minutes of mixing
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • waitWithin seconds
  • customa yellow precipitate formed
  • filtrationThe precipitate was filtered
  • customto remove
  • customthe reaction liquid
  • washwashed with 20 ml of chloroform resulting in pale yellow powder (1.45 g, 68% crude yield, mp=193° C.)
  • 출처 및 근거

    ORD 기록
    ord-7e32ce71c73e487bb45769959123f0b9
    출처 데이터셋
    uspto-grants-1995_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05401825

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