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HCID 59326823、化合物 → HCID 59326798、化合物

HRID 473668
ノート
印刷プレビュー

反応式

HRID 473668 の反応式
[F:1][C:2]1[C:7]([C:8]2[CH2:12][CH2:11][C:10](=[O:13])[CH:9]=2)=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:14][Mg]Br>C1COCC1.O>[F:1][C:2]1[C:7]([C:8]2[CH2:12][CH2:11][C:10]([CH3:14])([OH:13])[CH:9]=2)=[CH:6][CH:5]=[CH:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 59326823HCID 59326823、化合物HCID 178418573HCID 178418573、化合物

生成物 1

HCID 59326798HCID 59326798、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 3-(2-fluoropyridin-3-yl)cyclopent-2-enone (1 g, 5.64 mmol) in THF (28.2 mL) was added methylmagnesium bromide (4.70 mL, 14.11 mmol) dropwise over 5 minutes. The dark brown solution was stirred for 3 h at room temperature before. slowly quenching with aqueous ammonium chloride. The crude reaction was diluted with water and extracted with ethyl acetate, drying over magnesium sulfate, filtering, and concentrating to a dark brown oil under reduced pressure. The crude compound was purified by column chromatography (ethyl acetate/dichloromethane) to afford 3-(2-fluoropyridin-3-yl)-1-methylcyclopent-2-enol as a clear oil. MS (ESI, pos. ion) m/z: 194.1 (M+1).

後処理

  1. customslowly quenching with aqueous ammonium chloride
  2. customThe crude reaction
  3. extractionextracted with ethyl acetate
  4. dry with materialdrying over magnesium sulfate
  5. filtrationfiltering
  6. concentrationconcentrating to a dark brown oil under reduced pressure
  7. customThe crude compound was purified by column chromatography (ethyl acetate/dichloromethane)

出典と根拠

ORDレコード
ord-284533dd63ef4f728cfc39b5e49fc0da
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637500B2

反応ノート

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