用于有机合成。
有机合成
合成路线 1(1. 合成:19967-55-6)
产率:82%
合成条件:With sodium bicarbonate; calcium chloride; bromine In methanol; water
实验步骤:参考实施例4 2-苄氧基-N- [1-(3,5-二氯苯硫基)-3-甲基-2-氧代丁基] -N-甲基乙酰胺(20)的合成向300ml无水甲醇中加入43.1mg(0.5mol)称取3-甲基-2-丁酮,并将混合物在5℃下搅拌。在10℃下在30分钟内加入27.3ml(0.5mol)溴。在10℃下搅拌1小时后,加入150ml水,将混合物升温至室温并搅拌3小时。加入300毫升水后,混合物用500毫升乙醚萃取3次。萃取液用饱和碳酸氢钠水溶液洗涤,然后用饱和盐水洗涤,并将氯化钙加入到乙醚层中。将混合物搅拌1小时以脱水。过滤乙醚层,在低于30℃下浓缩,并在减压下蒸馏缩合物,得到67.49g的1-溴-3-甲基-2-丁酮(沸点67-75℃/ 28℃)。 mmHg,产率82%)。 1 H-NMR(CDCl 3 -TMS)δppm:1.18(d,J = 6.0Hz,6H),2.99(m,1H),4.00(s,2H)
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