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
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
- temperaturemaintaining the temperature below 30° C
- temperatureto cool to room temperature
- stirringthe mixture stirred
- extractionThe aqueous layer was extracted with diethyl ether (210 ml)
- dry with materialdried (MgSO4)
- concentrationThe solution was concentrated
- customto give 280 g of crude material
- custom140 g Of the crude was purified by chromatography on Biotage (800 g)
- 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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