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Methyl morpholine oxide → 2-Benzyl-2-azabicyclo[2.2.2]octan-6-one

HRID 1987239
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HRID 1987239 반응식
[CH2:1]([N:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[C@@H:10]([OH:16])[CH2:11]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[N+]1([O-])CCOCC1>C(#N)C.[Ru]([O-])(=O)(=O)=O.C([N+](CCC)(CCC)CCC)CC>[CH2:1]([N:8]1[CH2:13][CH:12]2[CH2:14][CH2:15][CH:9]1[C:10](=[O:16])[CH2:11]2)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 82029Methyl morpholine oxideHCID 2802928(6S)-2-Benzyl-2-azabicyclo[2.2.2]octan-6-OL

생성물 1

HCID 123174732-Benzyl-2-azabicyclo[2.2.2]octan-6-one수율 81%

시약·촉매·용매 2

HCID 178419074HCID 178419074, 화합물촉매HCID 6342Acetonitrile용매

실험 절차

To a vigorously stirring suspension of (6S)—N-benzyl-2-azabicyclo[2.2.2]octan-6-ol (1.5 g, 6.9 mmol, Maybridge) and activated 4 Å MS (1.0 g) in acetonitrile (70 mL) at 23° C. was sequentially added 4-methylmorpholine-N-oxide (1.2 g, 10 mmol) and tetrapropylammonium perruthenate (240 mg, 0.69 mmol). After stirring the resulting black suspension for 30 min, the mixture was concentrated in vacuo, and the resulting residue was purified by flash chromatography (20-50% ethyl acetate in hexanes) to provide N-benzyl-2-azabicyclo[2.2.2]octan-6-one as an orange oil (1.2 g, 81%). MS (AP CI) 216 (M+H).

후처리

  1. stirringAfter stirring the resulting black suspension for 30 min
  2. concentrationthe mixture was concentrated in vacuo
  3. customthe resulting residue was purified by flash chromatography (20-50% ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-423c56243d684bc58f31636106fb79c9
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07550500B2

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