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Tetrabutylammonium Hydroxide → Isohexane ethyl acetate

HRID 1443989
ノート
印刷プレビュー

反応式

HRID 1443989 の反応式
[OH-:1].[CH2:2]([N+](CC[CH2:17][CH3:18])(CCCC)CCCC)CCC.[Cl:19][C:20]1[C:25]([Cl:26])=[CH:24][CH:23]=[CH:22][C:21]=1[S:27]([N:30]([C:39]1[C:44]([O:45][CH3:46])=[N:43][C:42](Cl)=[C:41]([Cl:48])[N:40]=1)COCC[Si](C)(C)C)(=[O:29])=[O:28]>COCCOC.C(OCC)(=O)C>[C:44]([O:45][CH2:17][CH3:18])(=[O:1])[CH3:39].[CH3:22][CH2:23][CH2:24][CH:25]([CH3:20])[CH3:2].[Cl:19][C:20]1[C:25]([Cl:26])=[CH:24][CH:23]=[CH:22][C:21]=1[S:27]([NH:30][C:39]1[C:44]([O:45][CH3:46])=[N:43][C:42]([OH:1])=[C:41]([Cl:48])[N:40]=1)(=[O:29])=[O:28]
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 2

HCID 2723671Tetrabutylammonium HydroxideHCID 11180148HCID 11180148、化合物

生成物 2

HCID 21882781Isohexane ethyl acetateHCID 178494254HCID 178494254、化合物

試薬・触媒・溶媒 2

HCID 80711,2-Dimethoxyethane溶媒HCID 8857Ethyl Acetate溶媒

実験手順

tetrabutylammonium hydroxide (0.28 g of 40% aqueous solution) was added to a solution of 2,3-dichloro-N-(5,6-dichloro-3-methoxy-2-pyrazinyl)-N-{[2-(trimethylsilyl)ethoxy]methyl}benzenesulfonamide (0.25 g) in 1,2-dimethoxyethane (3.0 mL) at room temperature. After 16 h, the solution was diluted with ethyl acetate (20 mL). The organic solution was washed with aqueous citric acid (10 mL) and brine, dried (MgSO4) and evaporated. Chromatography on silica gel eluting with ethyl acetate/isohexane mixtures gave the title compound containing the SEM group, as a white solid (0.08 g). The solid was dissolved in trifluroacetic acid (2.0 mL) and dichloromethane (2.0 mL) and stirred at room temperature for 1 h. The reaction mixture was concentrated and chromatography on silica gel eluting with ethyl acetate/isohexane mixtures gave the title compound as a white solid (0.027 g).

後処理

  1. washThe organic solution was washed with aqueous citric acid (10 mL) and brine
  2. dry with materialdried (MgSO4)
  3. customevaporated

出典と根拠

ORDレコード
ord-2dc3ffcfe7e742dda562567b823bc21d
出典データセット
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07662825B2

反応ノート

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