反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A five liter, 3-necked, round-bottom flask equipped with a condenser plus scrubber, mechanical stirrer, and dropping funnel was used as the reaction vessel. The reaction vessel was cooled in an ice bath after charging with 1.2 liters of water. After the water had cooled, 126 ml (1.65 moles) of thiophosgene was added. The mixture was stirred vigorously while a solution containing 352 grams (1.52 moles) of 2-amino-5-chlorobenzophenone in about 1 liter of methylene chloride was added over a period of 20 to 25 minutes. After addition was complete the funnel was rinsed with about 150 ml of methylene chloride and the reaction mixture was stirred for about one hour with the ice bath in place. Then the ice bath was removed and the reaction mixture was stirred for one additional hour. The organic phase was separated, dried with magnesium sulfate, and concentrated in vacuo. The 2-benzoyl-4-chlorophenylisothiocyanate remained behind as a brown oil which solidified on cooling. The product was recrystallized from hexane to yield tan crystals.
WORKUP
后处理
- customA five liter, 3-necked, round-bottom flask equipped with a condenser
- temperatureThe reaction vessel was cooled in an ice bath
- additionwas added over a period of 20 to 25 minutes
- additionAfter addition
- washwas rinsed with about 150 ml of methylene chloride
- stirringthe reaction mixture was stirred for about one hour with the ice bath in place
- customThen the ice bath was removed
- stirringthe reaction mixture was stirred for one additional hour
- customThe organic phase was separated
- dry with materialdried with magnesium sulfate
- concentrationconcentrated in vacuo
- temperatureon cooling
- customThe product was recrystallized from hexane
- customto yield tan crystals