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Tetrabutylammonium Hydroxide → Isohexane ethyl acetate

HRID 1443989
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HRID 1443989 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 2723671Tetrabutylammonium HydroxideHCID 11180148HCID 11180148, 화합물

생성물 2

HCID 21882781Isohexane ethyl acetateHCID 178494254HCID 178494254, 화합물

시약·촉매·용매 2

HCID 80711,2-Dimethoxyethane용매HCID 8857Ethyl Acetate용매

실험 절차

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).

후처리

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

출처 및 근거

ORD 기록
ord-2dc3ffcfe7e742dda562567b823bc21d
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07662825B2

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