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Water → 4-(3-Hexyl-2-imidazolon-1-yl)phenylsulphonyl chloride

HRID 1736427
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HRID 1736427 반응식
CO[CH:3](OC)[CH2:4][NH:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[Cl:14][S:15]([C:18]1[CH:23]=[CH:22][C:21]([N:24]=[C:25]=[O:26])=[CH:20][CH:19]=1)(=[O:17])=[O:16].O.FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:6]([N:5]1[CH:4]=[CH:3][N:24]([C:21]2[CH:22]=[CH:23][C:18]([S:15]([Cl:14])(=[O:16])=[O:17])=[CH:19][CH:20]=2)[C:25]1=[O:26])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6422Trifluoroacetic acidHCID 81230p-Isocyanatobenzenesulphonyl chlorideHCID 59197986N-(2,2-dimethoxyethyl)hexan-1-amine

생성물 1

HCID 194205144-(3-Hexyl-2-imidazolon-1-yl)phenylsulphonyl chloride수율 67%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To the amine (38.6 mmol, 7.3 g) in methylene chloride (100 ml) at 0° C. was added 4-(chlorosulphonyl)phenyl isocyanate (38.6 mmol, 8.4 g). The reaction mixture was stirred for 20 mins until a clear solution had formed, and 1:1 water:trifluoroacetic acid (100 ml total) was added. Vigorous stirring was continued for 16 h., the layers separated, the organic layer was diluted with ethyl acetate (500 ml) and washed with saturated sodium bicarbonate solution (4×50 ml), brine (50 ml), dried with anhydrous magnesium sulphate, and concentrated in vacuo. Column chromatrography (eluant 3 hexane/1 ethyl acetate) yielded the title compound as pale yellow crystals (8.8 g, 67%).

후처리

  1. customhad formed
  2. stirringVigorous stirring
  3. waitwas continued for 16 h.
  4. customthe layers separated
  5. additionthe organic layer was diluted with ethyl acetate (500 ml)
  6. washwashed with saturated sodium bicarbonate solution (4×50 ml), brine (50 ml)
  7. dry with materialdried with anhydrous magnesium sulphate
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-52f9a11be44d48f18414ebdef9da42e4
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05541197

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