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Selectfluor → 3-Fluoro-1-(2-fluoro-4-nitrophenyl)piperidin-4-one

HRID 750906
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인쇄 미리보기

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HRID 750906 반응식
C[Si](C)(C)[O:3][CH:4]1[CH2:9][CH2:8][N:7]([C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][C:11]=2[F:19])[CH2:6][CH2:5]1.[B-](F)(F)(F)[F:23].[B-](F)(F)(F)F.C1[N+]2(CCl)CC[N+](F)(CC2)C1>C(#N)C>[F:23][CH:9]1[C:4](=[O:3])[CH2:5][CH2:6][N:7]([C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][C:11]=2[F:19])[CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2724933SelectfluorHCID 693102754-(4-Trimethylsilyloxy-piperidin-1-yl)-3-fluoronitrobenzene

생성물 1

HCID 597540583-Fluoro-1-(2-fluoro-4-nitrophenyl)piperidin-4-one수율 88%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

The mixture of 4-(4-trimethylsilyloxy-piperidin-1-yl)-3-fluoronitrobenzene (151 mmol), selectfluor (151 mmol) in acetonitrile was stirred for 4 hours. The solvent was removed under reduced pressure and to the residual mass was extracted into ethyl acetate water mixture. The combined organic layer was dried and removal of the solvent afforded title compound in 88% yield.

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후처리

  1. customThe solvent was removed under reduced pressure and to the residual mass
  2. extractionwas extracted into ethyl acetate water mixture
  3. customThe combined organic layer was dried
  4. customremoval of the solvent

출처 및 근거

ORD 기록
ord-236c3e1f308b4604a5d01d54f1f68fa7
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07405228B2

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