Propargyl alcohol → 3-(4-Fluorophenyl)prop-2-yn-1-ol
反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5](I)=[CH:4][CH:3]=1.[CH2:9]([OH:12])[C:10]#[CH:11].C(NC(C)C)(C)C>[Cu]I>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:11]#[C:10][CH2:9][OH:12])=[CH:4][CH:3]=1参加物
5
実験手順
To a mixture of 4-fluoroiodobenzene (710.0 mg, 3.82 mmol), bistriphenylphosphine palladium chloride (27.0 mg, 0.038 mmol), CuI (3.64 mg, 0.019 mmol) and propargyl alcohol (214.0 mg, 3.82 mmol), was added diisopropylamine (6.1 mL, 1.6 mL/mmol) under nitrogen atmosphere. The reaction mixture was stirred at r.t. for 6 h. After the completion of the reaction as confirmed by TLC, the crude product was extracted with ethylacetate (50 mL). The organic layer was washed with 10% HCl (20 mL), dried over Na2SO4 and concentrated in vacuo to afford the crude compound which was purified by column chromatography (silica gel, 2:8 EtOAc:Pet.Ether) to afford 3-(4-fluoro-phenyl)-prop-2-yn-1-ol (366.0 mg, 64%) as a viscous oil.
後処理
- customAfter the completion of the reaction
- extractionthe crude product was extracted with ethylacetate (50 mL)
- washThe organic layer was washed with 10% HCl (20 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customto afford the crude compound which
- customwas purified by column chromatography (silica gel, 2:8 EtOAc:Pet.Ether)
出典と根拠
- ORDレコード
- ord-4f4dbbfb635946ccbf5f9a823df32f63
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08455479B2
反応ノート
読み込み中…