Diethyl Ether → 1-Bromo-7-(prop-2-yn-1-yloxy)heptane

HRID 2118306

反応式

HRID 2118306 の反応式
[OH-].[Na+].[CH2:3]([OH:6])[C:4]#[CH:5].[Br:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]Br.C(OCC)C>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.O>[CH2:3]([O:6][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][Br:7])[C:4]#[CH:5]

参加物

7

反応条件

温度
60 °C

実験手順

25% (w/w) aq. NaOH (700 ml) was added to a stirred mixture of propargyl alcohol (70 g), tetra-butyl ammonium bromide (3.5 g) and 1,7-dibromoheptane (322 g) maintaining the temperature below 30° C. The reaction mixture was heated at 60° C. for 5 hrs then allowed to cool to room temperature and stirred overnight. Diethyl ether (350 ml) and water (280 m1) were added, the mixture stirred and allowed to settle. The aqueous layer was extracted with diethyl ether (210 ml), the organic layers combined, dried (MgSO4). The solution was concentrated to give 280 g of crude material. 140 g Of the crude was purified by chromatography on Biotage (800 g) eluting with petroleum ether then petroleum ether:ethyl acetate (100:1 followed by 100:1.5) to give the title compound (49.6 g).

後処理

  1. temperaturemaintaining the temperature below 30° C
  2. temperatureto cool to room temperature
  3. stirringthe mixture stirred
  4. extractionThe aqueous layer was extracted with diethyl ether (210 ml)
  5. dry with materialdried (MgSO4)
  6. concentrationThe solution was concentrated
  7. customto give 280 g of crude material
  8. custom140 g Of the crude was purified by chromatography on Biotage (800 g)
  9. washeluting with petroleum ether

出典と根拠

ORDレコード
ord-d80b0f33c29948bcb5784e1a1e5a2618
出典データセット
uspto-grants-2008_10
特許番号
US07442837B2

関連ノート

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