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Trifluoroacetic acid → 5-[(3,4-Dichlorophenyl)methyl]-2-azabicyclo[2.2.2]octane

HRID 1793640
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인쇄 미리보기

반응식

HRID 1793640 반응식
C(OC([N:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[CH2:10][CH:11]2[CH2:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[C:19]([Cl:24])[CH:18]=1)=O)(C)(C)C.ClCl.C(O)(C(F)(F)F)=O>>[Cl:24][C:19]1[CH:18]=[C:17]([CH:22]=[CH:21][C:20]=1[Cl:23])[CH2:16][CH:11]1[CH2:10][CH:9]2[CH2:15][CH2:14][CH:12]1[CH2:13][NH:8]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6422Trifluoroacetic acidHCID 24526ChlorineHCID 69593397HCID 69593397, 화합물

생성물 1

HCID 220228245-[(3,4-Dichlorophenyl)methyl]-2-azabicyclo[2.2.2]octane수율 96.8%

실험 절차

To a solution of 5-(3,4-dichloro-benzyl)-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid tert-butyl ester (0.24 g, 0.65 mmol) in 2 mL of CH2 Cl2 was added 1 mL of TFA. After the mixture was stirred at rt for 1 h, it was quenched with NaHCO3 (sat.). It was then extracted with CH2Cl2 and the organic layer was washed with NaCl (sat.), dried over Na2SO4 and concentrated to give 170 mg of 5-(3,4-Dichloro-benzyl)-2-aza-bicyclo[2.2.2]octane (M++1: 270).

후처리

  • customit was quenched with NaHCO3 (sat.)
  • extractionIt was then extracted with CH2Cl2
  • washthe organic layer was washed with NaCl (sat.)
  • dry with materialdried over Na2SO4
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-44ae9cae3c594257b3e75c823ab048f1
    출처 데이터셋
    uspto-grants-2006_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07081531B2

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