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

HRID 863801
ノート
印刷プレビュー

反応式

HRID 863801 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

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:trifiuoroacetic acid (100 ml total) was added. Vigorous stirring was continued for 16h., 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%).

後処理

  1. customhad formed
  2. stirringVigorous stirring
  3. waitwas continued for 16h.
  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

出典と根拠

ORDレコード
ord-4b5d44bbbd9b426d99c184a49a22c12c
出典データセット
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05561142

反応ノート

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