反応 #213890
ord-587ca881898b4c73b3c1b4c9974535a8
反応方程式
反応物
試薬
反応条件
後処理
- 1workup.ADDITIONTo a suspension of 5.31 g
- 2workup.ADDITIONfollowed by the dropwise addition of a solution of 25 g
- 3workup.ADDITIONMidway through the addition 15 ml
- 4workup.ADDITIONAfter complete addition of the solution
- 5温度the mixture is refluxed for 40 minutes
- 6ろ過The mixture is filtered through Celite
- 7その他the solvent is removed
- 8workup.DISSOLUTIONThe residue is dissolved in 53 ml
- 9workup.ADDITIONof dimethylformamide and at 0° C. is added 24.4 g
- 10抽出extracted with hexanes
- 11乾燥The organic layer is dried over magnesium sulfate
- 12その他the solvent is removed
- 13workup.DISTILLATIONDistillation (75°-95° C., 0.3 mm.)
- 14その他gives 17.4 g
実験手順
To a suspension of 5.31 g. (0.22 moles) of magnesium in 15 ml. of ether is added 100 mg. of mercuric chloride and 1.5 ml. of 1,2-dibromoethane. After the reaction begins, another 45 ml. of ether is added followed by the dropwise addition of a solution of 25 g. (0.16 moles of 1,1-dimethoxy-2-hexanone and 27.3 g. (0.2 moles) of 85% propargyl bromide in 45 ml. of ether at a rate which maintains reflux. Midway through the addition 15 ml. of tetrahydrofuran is added. After complete addition of the solution, the mixture is refluxed for 40 minutes. The mixture is cooled to 0° C. and saturated ammonium chloride solution is added followed by magnesium sulfate. The mixture is filtered through Celite and the solvent is removed. The residue is dissolved in 53 ml. of dimethylformamide and at 0° C. is added 24.4 g. (0.36 moles) of imidazole and 21.19 g. (0.20 moles) of trimethylchlorosilane. After stirring at 25° C. for 70 minutes, the solution is poured into water and extracted with hexanes. The organic layer is dried over magnesium sulfate and the solvent is removed. Distillation (75°-95° C., 0.3 mm.) gives 17.4 g. of the title compound.