反応式
[Mg].[CH2:2](Cl)[C:3](=[CH2:5])[CH3:4].[C:7]([CH:10]1[C:15]([CH3:17])([CH3:16])[CH:14]2[CH2:18][CH:11]1[CH:12]=[CH:13]2)(=[O:9])[CH3:8].[Cl-].[NH4+]>C(OCC)C>[CH2:2]([C:7]([CH3:8])([CH:10]1[C:15]([CH3:16])([CH3:17])[CH:14]2[CH2:18][CH:11]1[CH:12]=[CH:13]2)[OH:9])[C:3](=[CH2:5])[CH3:4]参加物
実験手順
Into a 1 liter reaction flask equipped with a reflux condenser, thermometer, stirrer, dropping funnel and nitrogen inlet tube are placed 12 g (0.5 moles) of magnesium turnings and 250 cc anhydrous diethyl ether. Over a 2 hour period, 45.3 g (0.5 moles) of methallyl chloride is added. The Grignard solution is stirred for 1/2 hour and 28 g of 2-acetyl-3,3-dimethyl-5-norbornene is added over a 20 minute period. The mixture is stirred at reflux for 1/2 hour and then is hydrolyzed by the addition of saturated ammonium chloride solution. The organic layer is washed with water and dried over magnesium sulfate. The mixture is then filtered and the solvent evaporated to yield 40 g of an oil, which is then fractionated on a micro Vigreux column after adding thereto 5 g Primol® and a trace quantity of Ionox®.
後処理
- customInto a 1 liter reaction flask
- customequipped with a reflux condenser
- customthermometer, stirrer, dropping
- customfunnel and nitrogen inlet tube are placed
- stirringThe mixture is stirred
- temperatureat reflux for 1/2 hour
- washThe organic layer is washed with water
- dry with materialdried over magnesium sulfate
- filtrationThe mixture is then filtered
- customthe solvent evaporated
出典と根拠
- ORDレコード
- ord-8d98939ba4254bfdae96417e380f1482
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04148826
関連ノート
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