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Boron trifluoride etherate → Diethyl 5-oxoazepane-1,4-dicarboxylate

HRID 2353047
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HRID 2353047 반응식
[C:1]([N:6]1[CH2:11][CH2:10][C:9](=[O:12])[CH2:8][CH2:7]1)([O:3][CH2:4][CH3:5])=[O:2].B(F)(F)F.[CH3:17]COCC.[N+]([C:27]([O:29][CH2:30][CH3:31])=[O:28])(C([O-])=O)=[N-]>CCOCC>[O:12]=[C:9]1[CH2:10][CH2:11][N:6]([C:1]([O:3][CH2:4][CH3:5])=[O:2])[CH2:17][CH2:7][CH:8]1[C:27]([O:29][CH2:30][CH3:31])=[O:28]
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참가 물질

5

반응물 3

HCID 8000Boron trifluoride etherateHCID 34767Ethyl 4-oxo-1-piperidinecarboxylateHCID 86610729Ethyl diazodicarboxylate

생성물 1

HCID 12485293Diethyl 5-oxoazepane-1,4-dicarboxylate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

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온도
-30 °C

실험 절차

To a cold solution (−30° C.) of 1-carbethoxypiperidin-4-one (3.0 ml, 26.5 mmol) in anhydrous ether, were simultaneously added a solution of boron trifluoride etherate (3.4 ml, 26.5 mmol) in diethyl ether (2.8 ml) and a solution of ethyl diazodicarboxylate (3.6 ml, 34.5 mmol) in diethyl ether (2.8 ml) over 1.5 hours via a syringe-pump. Upon completion of additions, the reaction mixture was allowed to stir for an additional hour at −30° C. and then warmed to room temperature. The reaction mixture was washed with 30% potassium carbonate and the organic phase was dried over Na2SO4 and concentrated in vacuo to give diethyl 5-oxoazepane-1,4-dicarboxylate as a crude yellow oil.

후처리

  1. temperaturewarmed to room temperature
  2. washThe reaction mixture was washed with 30% potassium carbonate
  3. dry with materialthe organic phase was dried over Na2SO4
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-7b69eb52042141b5b90c6e0f25005880
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07749994B2

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