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Allyl bromide → (Pent-4-en-1-yl)benzene

HRID 1380125
ノート
印刷プレビュー

反応式

HRID 1380125 の反応式
[CH2:1]([Mg]Br)[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:11](Br)[CH:12]=[CH2:13]>O1CCCC1>[C:3]1([CH2:2][CH2:1][CH2:13][CH:12]=[CH2:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 7841Allyl bromideHCID 178419670HCID 178419670、化合物

生成物 1

HCID 517892(Pent-4-en-1-yl)benzene

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of phenethyl magnesium bromide (prepared from 25 l g, 0.135 mol of phenethyl bromide and excess magnesium turnings) in anhydrous tetrahydrofuran (50 ml) was added to a stirred solution of allyl bromide (16.34 g, 0.135 mol) in anhydrous tetrahydrofuran (150 ml) at room temperature and under an atmosphere of dry nitrogen. The mixture was stirred at room temperature for 3 hours and the solvent was then evaporated off under reduced pressure and the residue was dissolved in ethyl acetate. The solution was washed with a saturated aqueous solution of ammonium chloride and the solvent was evaporated off under reduced pressure to give an oil which was distilled to give 5-phenylpent-1-ene as a colourless oil (b.p. 40° C., 0.5 mm, Hg).

後処理

  1. customthe solvent was then evaporated off under reduced pressure
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washThe solution was washed with a saturated aqueous solution of ammonium chloride
  4. customthe solvent was evaporated off under reduced pressure
  5. customto give an oil which
  6. distillationwas distilled

出典と根拠

ORDレコード
ord-f8358a5990264efc818245dcb3d19efe
出典データセット
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04579862

反応ノート

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