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Triethylamine → HCID 86735078, 화합물

HRID 2072026
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HRID 2072026 반응식
Cl[CH:2]([CH2:5][S:6]([C:9]1[CH:14]=[CH:13][C:12]([O:15][C:16]([F:21])([F:20])[CH:17]([Cl:19])[Cl:18])=[CH:11][CH:10]=1)(=[O:8])=[O:7])C#N.[CH2:22]([N:24](CC)CC)C>C1C=CC=CC=1>[Cl:19][CH:17]([Cl:18])[C:16]([F:20])([F:21])[O:15][C:12]1[CH:11]=[CH:10][C:9]([S:6]([C:5](=[CH2:2])[C:22]#[N:24])(=[O:7])=[O:8])=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8471TriethylamineHCID 20310058HCID 20310058, 화합물

생성물 1

HCID 86735078HCID 86735078, 화합물

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

To 3.0 g (0.079 mol) of 2-chloro-3-((4-(2,2-dichloro-1,1-difluoroethoxy)phenyl)sulfonyl)propanenitrile in 100 ml of benzene was added a slight molar excess of triethylamine. The reaction mixture was filtered to remove the triethylamine hydrochloride produced. The benzene was removed in vacuo from the filtrate, and the residue which remained was crystallized from methanol/ water to give 1.5 g of the title compound as a tan solid, mp 89°-90° C.

후처리

  1. filtration
The reaction mixture was filtered
  • customto remove the triethylamine hydrochloride
  • customproduced
  • customThe benzene was removed in vacuo from the filtrate
  • customthe residue which remained was crystallized from methanol/ water
  • 출처 및 근거

    ORD 기록
    ord-87ae05ab13dc4813a7490c4f1190b628
    출처 데이터셋
    uspto-grants-1977_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04049696

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