Environment friendly method for preparing bromopropane
An environmentally friendly, bromopropane technology, applied in the preparation of halogenated hydrocarbons, chemical instruments and methods, organic chemistry, etc., can solve the problems of high production cost, poor recycling, low content, etc., to reduce production safety hazards, The effect of ensuring occupational safety and health and being easy for industrial application
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Embodiment 1
[0027] In a four-necked flask equipped with a condensation collection device, a stirrer, a thermometer and a constant pressure dropping funnel, add 200 g of 48% (mass concentration, the same below) hydrobromic acid (accounting for about 1 / 5 of the volume of the container), and start Stir the device, and heat up, weigh 685g of 48% hydrobromic acid and 247g of 99% propanol simultaneously, the two are uniformly mixed and placed in the constant pressure dropping funnel. Prepare saturated aqueous sodium carbonate solution. When the temperature in the four-neck flask rises to 108°C, open the constant pressure dropping funnel and drop the mixed solution at a constant speed, raise the temperature to keep the temperature in the flask at 120-125°C, open the condenser to cool down and receive bromopropane. The bromopropane crude product was left to rest for 2 hours, and the layers were separated. The lower oil phase was washed with a saturated aqueous solution of sodium carbonate to a pH...
Embodiment 2
[0029] In a four-necked flask equipped with a condensation collecting device, a stirrer, a thermometer and a constant pressure dropping funnel, add 300 g of 40% hydrobromic acid (accounting for about 1 / 3 of the volume of the container), start the stirring device, and heat up, while Weigh 822g of 40% hydrobromic acid and 257g of 95% propanol to prepare saturated aqueous sodium carbonate solution. When the temperature in the four-neck flask rises to 115°C, hydrobromic acid and propanol solution are added dropwise at the same time (to ensure that HBr and CH 3 CH 2 CH 2 The feed molar ratio of OH is 1:1), the temperature is raised to keep the temperature in the bottle at 125-130°C, and bromopropane is received by condensation. The bromopropane crude product was left to rest for 1.5 hours, separated into layers, and the lower oil phase was washed with a saturated aqueous solution of sodium carbonate to a pH value of 8, and washed twice with water to a pH value of 7, and dried ove...
Embodiment 3
[0031] In a four-necked flask equipped with a condensation collection device, a stirrer, a thermometer and a constant pressure dropping funnel, add 300 g of 49% hydrobromic acid (accounting for about 1 / 3 of the volume of the container), start the stirring device, and heat up. Simultaneously weigh 438g of 60% hydrobromic acid and 197g of 99% propanol and mix uniformly to prepare saturated aqueous sodium carbonate solution. When the temperature in the four-neck flask rises to 120°C, add the mixture of hydrobromic acid and propanol solution dropwise, raise the temperature to keep the temperature in the flask at 130-135°C, and condense to receive bromopropane. The bromopropane crude product was left to rest for 3 hours, and the layers were separated. The lower oil phase was washed with a saturated aqueous sodium carbonate solution and the pH value was 8, and washed twice with water, and the pH value was 7. After drying with molecular sieves, bromopropane was obtained with a yield o...
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