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Propargyl alcohol → 3-(3-fluorophenyl)prop-2-yn-1-ol

HRID 889001
ノート
印刷プレビュー

反応式

HRID 889001 の反応式
[CH2:1]([OH:4])[C:2]#[CH:3].[F:5][C:6]1[CH:7]=[C:8](I)[CH:9]=[CH:10][CH:11]=1>[Cu](I)I.C(NCC)C>[F:5][C:6]1[CH:11]=[C:10]([C:3]#[C:2][CH2:1][OH:4])[CH:9]=[CH:8][CH:7]=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

5

反応物 2

HCID 7859Propargyl alcoholHCID 707251-Fluoro-3-iodobenzene

生成物 1

HCID 27826973-(3-fluorophenyl)prop-2-yn-1-ol収率 93%

試薬・触媒・溶媒 2

HCID 83717Copper iodide触媒HCID 8021Diethylamine溶媒

反応条件

温度
25 °C

実験手順

A mixture of propargyl alcohol (0.200 g, 5.4 mmol), 3-fluoro iodobenzene (0.63 ml, 5.4 mmol), copper iodide (0.103 g, 0.54 mol), dichlorobis (triphenylphosphine) palladium (II) (0.190 g, 0.3 mmol), diethylamine (10 ml) was degassed for 10 min. and stirred for 20 hrs at 25-25° C. Excess of diethyl amine was distilled off under vacuum. The residue was diluted with water (10 ml) and extracted with ethyl acetate. The organic layer was washed with brine solution and dried over Na2SO4. The solvent was evaporated and the crude product was purified by column chromatography (10% Ethyl acetate in hexane) to obtain pure 3-(3-fluoro-phenyl)-prop-2-yn-1-ol (0.750 g, 93%).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. customwas degassed for 10 min.
  2. distillationExcess of diethyl amine was distilled off under vacuum
  3. additionThe residue was diluted with water (10 ml)
  4. extractionextracted with ethyl acetate
  5. washThe organic layer was washed with brine solution
  6. dry with materialdried over Na2SO4
  7. customThe solvent was evaporated
  8. customthe crude product was purified by column chromatography (10% Ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-b4b81e05f590466c97e4a268ba559317
出典データセット
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08252797B2

反応ノート

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