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

HRID 1824960
ノート
印刷プレビュー

反応式

HRID 1824960 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 713FormamideHCID 10942334Sodium MethoxideHCID 22144818HCID 22144818、化合物

生成物 1

HCID 221448132-(5-Fluorobenzofur-7-yl)propionamide収率 25%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
100 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-813138b3309c42589e021090076a0b54
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07045545B1

反応ノート

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