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Formamide → 2-(5-Fluorobenzofur-7-yl)propionamide

HRID 1824960
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HRID 1824960 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:11]([CH3:17])[C:12](OCC)=[O:13])[C:5]2[O:9][CH:8]=[CH:7][C:6]=2[CH:10]=1.C([NH2:20])=O.C[O-].[Na+]>CN(C)C=O.C(OCC)(=O)C>[F:1][C:2]1[CH:3]=[C:4]([CH:11]([CH3:17])[C:12]([NH2:20])=[O:13])[C:5]2[O:9][CH:8]=[CH:7][C:6]=2[CH:10]=1
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참가 물질

6

반응물 3

HCID 713FormamideHCID 10942334Sodium MethoxideHCID 22144818HCID 22144818, 화합물

생성물 1

HCID 221448132-(5-Fluorobenzofur-7-yl)propionamide수율 25%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 8857Ethyl Acetate용매

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온도
100 °C

실험 절차

To a solution of 0.27 gm (1.15 mMol) ethyl 2-(5-fluorobenzofur-7-yl)propionate in 4 mL dimethylformamide were added sequentially 0.16 mL (3.91 mMol) freshly distilled formamide and 0.81 mL (0.80 mMol) sodium methoxide (1 M in methanol) dropwise and the resulting mixture was heated at 100° C. for 45 minutes. The reaction mixture was cooled to room temperature and was then diluted with 25 volumes of ethyl acetate. The mixture was then washed sequentially with water and saturated aqueous sodium chloride, and concentrated under reduced pressure. The residue was subjected to flash silica gel chromatography, eluting with 2:1 ethyl acetate:hexane. Fractions containing product were combined and concentrated under reduced pressure to provide 0.060 gm (25%) of the desired compound.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. washThe mixture was then washed sequentially with water and saturated aqueous sodium chloride
  3. concentrationconcentrated under reduced pressure
  4. washeluting with 2:1 ethyl acetate
  5. additionFractions containing product
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-813138b3309c42589e021090076a0b54
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045545B1

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