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Phosphorus tribromide → 1-(3-Bromopropyl)-4-methoxybenzene

HRID 496083
ノート
印刷プレビュー

反応式

HRID 496083 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11]O)=[CH:5][CH:4]=1.P(Br)(Br)[Br:14]>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][Br:14])=[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 24614Phosphorus tribromideHCID 794063-(4-Methoxyphenyl)-1-propanol

生成物 1

HCID 127769961-(3-Bromopropyl)-4-methoxybenzene収率 61.1%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution of 3-(p-methoxyphenyl)-1-propanol (16.6 g; 0.1 mol) in 250 ml of toluene, cooled to 0° C., was added dropwise 26 ml of phosphorus tribromide (0.27 mol). Following completion of the addition, the reaction was stirred at room temperature for 1 hour, then refluxed for an additional hour. The reaction was cooled and poured onto ice, the layers were separated, and the organic phase washed with saturated sodium bicarbonate (3×) and brine (3×). The crude material obtained upon drying and evaporation of the solvent was chromatographed, eluting with 10% EtOAc/hexane, to obtain 14 g (61%) of 3-(p-methoxyphenyl)-1-propylbromide.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additioncompletion of the addition
  2. temperaturerefluxed for an additional hour
  3. temperatureThe reaction was cooled
  4. additionpoured onto ice
  5. customthe layers were separated
  6. washthe organic phase washed with saturated sodium bicarbonate (3×) and brine (3×)
  7. customThe crude material obtained
  8. customupon drying
  9. customevaporation of the solvent
  10. customwas chromatographed
  11. washeluting with 10% EtOAc/hexane

出典と根拠

ORDレコード
ord-c050fe7f835445ce943decc00f6cc90b
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06943187B2

反応ノート

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