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2-Chloro-4-fluorobenzonitrile → HCID 17986305, 화합물

HRID 2233386
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HRID 2233386 반응식
CC(C)([O-])C.[K+].[OH:7][CH:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:10][CH2:9]1.[Cl:21][C:22]1[CH:29]=[C:28](F)[CH:27]=[CH:26][C:23]=1[C:24]#[N:25]>C(COC)OC>[Cl:21][C:22]1[CH:29]=[C:28]([CH:27]=[CH:26][C:23]=1[C:24]#[N:25])[O:7][CH:8]1[CH2:9][CH2:10][N:11]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[CH2:12][CH2:13]1
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참가 물질

5

반응물 3

HCID 1090002-Chloro-4-fluorobenzonitrileHCID 643502Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 23665647Potassium tert-butoxide

생성물 1

HCID 17986305HCID 17986305, 화합물수율 41.2%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

실험 절차

Potassium tert-butoxide (5.57 g, 49.68 mmol) was added to a solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (5.00 g, 24.84 mmol) in glyme (100 ml) and the mixture stirred for 30 min. before addition of 2 chloro-4-fluoro-benzonitrile (7.73 g, 49.68 mmol). The reaction was stirred at room temperature overnight and then partitioned between ethyl acetate (250 ml) and water (200 ml). The organic layer was separated, dried over magnesium sulfate and the solvent evaporated. The residue was purified by flash chromatography eluting with ethyl acetate:isohexane (4:1) to give the subtitle compound as a colourless solid (3.45 g).

후처리

  1. custompartitioned between ethyl acetate (250 ml) and water (200 ml)
  2. customThe organic layer was separated
  3. dry with materialdried over magnesium sulfate
  4. customthe solvent evaporated
  5. customThe residue was purified by flash chromatography
  6. washeluting with ethyl acetate:isohexane (4:1)

출처 및 근거

ORD 기록
ord-98663181b051448f92def660614d2967
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709500B2

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