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2-Propylphenol → 4-Bromo-2-propylphenol

HRID 858609
ノート
印刷プレビュー

反応式

HRID 858609 の反応式
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH2:2][CH3:3].[Br-:11].[Br-].[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC.C([N+](CCCC)(CCCC)CCCC)CCC>C(Cl)(Cl)Cl>[Br:11][C:8]1[CH:7]=[CH:6][C:5]([OH:10])=[C:4]([CH2:1][CH2:2][CH3:3])[CH:9]=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 125702-PropylphenolHCID 23500184Tetra-n-butylammonium tribromide

生成物 1

HCID 221345104-Bromo-2-propylphenol

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

実験手順

2-propylphenol (3.0 g, 0.022 mol) was dissolved in CHCl3 (100 mL) and magnetically stirred at room temperature. To this solution was added a solution of Tetrabutyl ammonium tribromide (10.68 g, 0.022 mol) in CHCl3 (100 mL). The resulting yellow solution was allowed to stir at room temperature for 1 hour. The reaction was quenched with a 5% solution of sodium thiosulfate (200 mL). The biphasic mixture was stirred for 15 min. The organics were separated and concentrated. The residue was dissolved in EtOAc (100 mL) and washed with water (2×100 mL) and brine (1×100 mL). The organics were dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography (silica gel) eluting with 3% EtOAc in Hexanes. The result was a yellow oil (4.54 g).

後処理

  1. stirringto stir at room temperature for 1 hour
  2. customThe reaction was quenched with a 5% solution of sodium thiosulfate (200 mL)
  3. stirringThe biphasic mixture was stirred for 15 min
  4. customThe organics were separated
  5. concentrationconcentrated
  6. dissolutionThe residue was dissolved in EtOAc (100 mL)
  7. washwashed with water (2×100 mL) and brine (1×100 mL)
  8. dry with materialThe organics were dried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe residue was purified by flash chromatography (silica gel)
  12. washeluting with 3% EtOAc in Hexanes

出典と根拠

ORDレコード
ord-c7aef61e419f4af4b363fe7a32ded9ab
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07148226B2

反応ノート

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