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
CONDITIONS
反应条件
- 温度
- 155 °C
PROCEDURE
实验过程
Into the column described in Example 1 were charged 453 grams (3.58 moles) of o-chlorotoluene, 2.25 grams of cobalt octoate (6% Co), and 2.25 grams of epichlorohydrin. The reaction mixture was heated to 155° C. and maintained at that temperature while oxygen that had been sparged through epichlorohydrin was bubbled through it at the rate of 200 ml./min. Throughout the reaction period, the gases leaving the reactor remained non-acidic. At the end of 23 hours, the reaction mixture was removed from the column, cooled to 75° C., and extracted with 600 grams of 10 percent aqueous sodium hydroxide solution. The layers that formed were separated. The aqueous layer was diluted with water to a volume of 1500 ml. and then acidified with hydrochloric acid. The o-chlorobenzoic acid that precipitated was collected, washed with water, and dried. There was obtained 180 grams (1.155 moles) of o-chlorobenzoic acid. The conversion of o-chlorotoluene to o-chlorobenzoic acid was 14 percent. The yield of o-chlorobenzoic acid, based on o-chlorotoluene reacted, was 78.6 percent.
WORKUP
后处理
- customhad been sparged through epichlorohydrin
- customwas bubbled through it at the rate of 200 ml
- customThroughout the reaction period
- customthe gases leaving the reactor
- customAt the end of 23 hours, the reaction mixture was removed from the column
- temperaturecooled to 75° C.
- extractionextracted with 600 grams of 10 percent aqueous sodium hydroxide solution
- customThe layers that formed
- customwere separated
- additionThe aqueous layer was diluted with water to a volume of 1500 ml
- customThe o-chlorobenzoic acid that precipitated
- customwas collected
- washwashed with water
- customdried