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Water → HCID 90022866, 화합물

HRID 56256
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HRID 56256 반응식
[F:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[H-].[Na+].Br[CH2:12][C:13](=[O:31])[CH2:14][C:15]([NH:17][C:18]1[CH:23]=[CH:22][C:21]([N:24]2[CH2:29][CH2:28][O:27][CH2:26][CH2:25]2)=[C:20]([F:30])[CH:19]=1)=[O:16].O>C1COCC1>[F:30][C:20]1[CH:19]=[C:18]([NH:17][C:15](=[O:16])[CH2:14][C:13](=[O:31])[CH2:12][O:8][C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[CH:3]=2)[CH:23]=[CH:22][C:21]=1[N:24]1[CH2:25][CH2:26][O:27][CH2:28][CH2:29]1
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반응물 4

HCID 962WaterHCID 97433-FluorophenolHCID 24758Sodium hydrideHCID 900232464-bromo-N-(3-fluoro-4-morpholinophenyl)-3-oxobutanamide

생성물 1

HCID 90022866HCID 90022866, 화합물수율 2.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 3-fluorophenol (2.33 g, 20.8 mmol) in anhydrous THF (20 mL) was added NaH (909 mg, 22.7 mmol, 60%) and the mixture was stirred at rt for 3 h. A solution of 4-bromo-N-(3-fluoro-4-morpholinophenyl)-3-oxobutanamide (6.8 g, 18.9 mmol) in THF (40 mL) was added. The resulting mixture was stirred at rt overnight. The reaction mixture was then poured into 100 mL of water and the mixture was extracted with EtOAc (30 mL×5). The combined organic phases were washed with brine (50 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=2:1) to give the title compound as a yellow solid (0.16 g, 2%).

후처리

  1. stirringThe resulting mixture was stirred at rt overnight
  2. extractionthe mixture was extracted with EtOAc (30 mL×5)
  3. washThe combined organic phases were washed with brine (50 mL×2)
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=2:1)

출처 및 근거

ORD 기록
ord-8449c024cad64d188bb9f1be4ab5c53b
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434695B2

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