Water → (5-Bromopentyl)benzene

HRID 397846

反応式

HRID 397846 の反応式
P(Br)(Br)[Br:2].[C:5]1([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]O)[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.O>O1CCOCC1.C(OCC)(=O)C>[Br:2][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

参加物

6

実験手順

Phosphorus tribromide (4.7 ml, 49.8 mmol) was added dropwise to a solution of 5-phenylpentan-1-ol (3 ml, 17.8 mmol) in dioxane (70 ml). The reaction mixture was stirred for 2 hours at room temperature. Another portion of phosphorus tribromide (4.7 m. 49.8 mmol) was added. The reaction mixture was stirred for 16 h at room temprature. It was cooled to 0° C. Water (60 ml) was added dropwise. The reaction mixture was diluted with ethyl acetate (100 ml). The phases were separated. The aqueous phase was extracted with ethyl acetate (2×100 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml) and dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (50 g), using ethyl acetate/heptane (1:10) as eluent, to give 1.35 g of 1-bromo-5-phenylpentane.

後処理

  1. stirringThe reaction mixture was stirred for 16 h at room temprature
  2. temperatureIt was cooled to 0° C
  3. customThe phases were separated
  4. extractionThe aqueous phase was extracted with ethyl acetate (2×100 ml)
  5. washThe combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml)
  6. dry with materialdried over magnesium sulfate
  7. customThe solvent was removed in vacuo
  8. customThe crude product was purified by flash chromatography on silica (50 g)

出典と根拠

ORDレコード
ord-bc7972ff90b545cba67eccff77153a1f
出典データセット
uspto-grants-2003_08
特許番号
US06610721B2

関連ノート

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