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Allyl isocyanate → N-[2-(1,2-dichlorovinyloxy)phenylsulfonyl]-N'-allylurea

HRID 638638
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HRID 638638 반응식
[CH2:1]([N:4]=[C:5]=[O:6])[CH:2]=[CH2:3].[Cl:7][C:8]([O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[S:18]([NH2:21])(=[O:20])=[O:19])=[CH:9][Cl:10].N12CCCN=C1CCCCC2>C(Cl)Cl>[Cl:7][C:8]([O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[S:18]([NH:21][C:5]([NH:4][CH2:1][CH:2]=[CH2:3])=[O:6])(=[O:19])=[O:20])=[CH:9][Cl:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 15123Allyl isocyanateHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 537128512-[(1,2-Dichloroethenyl)oxy]benzene-1-sulfonamide

생성물 1

HCID 53916718N-[2-(1,2-dichlorovinyloxy)phenylsulfonyl]-N'-allylurea

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 3.3. g of allyl isocyanate in 10 ml of methylene chloride is added dropwise to a mixture of 10.7 g of 2-(1,2-dichlorovinyloxy)phenylsulfonamide and 6.1 g of 1,8-diazabicyclo[5.4.0]undec-7-ene in 100 ml of methylene chloride, with stirring. When the exothermic reaction has subsided, stirring of the reaction mixture is continued at 20° to 25° C. for a further hour and the solvent is then evaporated off. The residue is dissolved in 5% sodium carbonate solution. The solution is filtered and acidified with 10% hydrochloric acid, whereupon the product precipitates as crystals. After filtration and drying, 13.2 g of N-[2-(1,2-dichlorovinyloxy)phenylsulfonyl]-N'-allylurea are obtained. Melting point: 187°-188° C.

후처리

  1. customWhen the exothermic reaction
  2. stirringstirring of the reaction mixture
  3. waitis continued at 20° to 25° C. for a further hour
  4. customthe solvent is then evaporated off
  5. dissolutionThe residue is dissolved in 5% sodium carbonate solution
  6. filtrationThe solution is filtered
  7. customprecipitates as crystals
  8. filtrationAfter filtration
  9. customdrying

출처 및 근거

ORD 기록
ord-f69afe56f2fb4f319f4a34d0a1747d0d
출처 데이터셋
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04562210

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