Propargyl alcohol → 3-(4-Fluorophenyl)prop-2-yn-1-ol

HRID 1253899노트

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HRID 1253899 반응식
[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

참가 물질

5

실험 절차

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.

후처리

  1. customAfter the completion of the reaction
  2. extractionthe crude product was extracted with ethylacetate (50 mL)
  3. washThe organic layer was washed with 10% HCl (20 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customto afford the crude compound which
  7. customwas purified by column chromatography (silica gel, 2:8 EtOAc:Pet.Ether)

출처 및 근거

ORD 기록
ord-4f4dbbfb635946ccbf5f9a823df32f63
출처 데이터셋
uspto-grants-2013_06
특허 번호
US08455479B2

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