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Trifluoroacetic acid → 3-(3,4-Dichloro-benzyl)-8-aza-bicyclo[3.2.1]octane

HRID 1793644
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반응식

HRID 1793644 반응식
C(OC([N:8]1[CH:13]2[CH2:14][CH2:15][CH:9]1[CH2:10][CH:11]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[C:19]([Cl:24])[CH:18]=1)[CH2:12]2)=O)(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[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[NH:8][CH:13]([CH2:14][CH2:15]2)[CH2:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 69593412HCID 69593412, 화합물

생성물 1

HCID 220228273-(3,4-Dichloro-benzyl)-8-aza-bicyclo[3.2.1]octane수율 98.4%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3-(3,4-Dichloro-benzyl)-8-aza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (0.35 g, 0.94 mmol) was stirred in 2 mL of CH2Cl2 with 0.5 mL of TFA at rt for 3 h. After being quenched with 20% NaOH to basic medium, the mixture was extracted with EtOAc. The organic layer was washed with NaCl (sat.), dried over Na2SO4 and concentrated to give 0.25 g of 3-(3,4-Dichloro-benzyl)-8-aza-bicyclo[3.2.1]octane.

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후처리

  1. customAfter being quenched with 20% NaOH to basic medium
  2. extractionthe mixture was extracted with EtOAc
  3. washThe organic layer was washed with NaCl (sat.)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-cc5d6d3efe544eaeb49452f7c8ca9b47
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07081531B2

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