Synthetic method for N,N-dicyclohexylamine-2-butanol
A technology of dicyclohexylamine and a synthesis method, which is applied in the synthesis field of N,N-dicyclohexylamine-2-butanol, can solve the problems of few product varieties and limited application coverage, etc., and achieves inhibition of corrosion, improvement of Effect of anodic polarization properties
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Embodiment 1
[0012] In a four-neck flask equipped with a stirring device, a reflux condensing device and a thermometer, add 36.5 grams of cyclohexane, add 2.5 grams of zinc chloride and 33 grams of dicyclohexylamine, and slowly add 11 grams of butylene oxide under stirring conditions , reflux at 80°C to 85°C for 8 hours to generate N,N-dihydroxyisopropylcyclohexylamine. After the reaction is completed, the solvent and unreacted substances are distilled off under reduced pressure, and the product is purified by gel chromatography. Elution was carried out three times with acetone-ethyl acetate at a volume ratio of 20:30 to obtain N,N-dicyclohexylamine-2-butanol as a colorless liquid.
Embodiment 2
[0014] In a four-necked flask equipped with a stirring device, a reflux condensing device and a thermometer, add 43 grams of cyclohexane, add 4 grams of zinc chloride and 36 grams of dicyclohexylamine, and slowly add 11.5 grams of butylene oxide under stirring conditions , reflux at 85°C to 90°C for 7 hours to generate N,N-dihydroxyisopropylcyclohexylamine. After the reaction is completed, the solvent and unreacted substances are distilled off under reduced pressure, and the product is purified by gel chromatography. Elution was carried out three times with acetone-ethyl acetate at a volume ratio of 20:30 to obtain N,N-dicyclohexylamine-2-butanol as a colorless liquid.
Embodiment 3
[0016] In a four-necked flask equipped with a stirring device, a reflux condensing device and a thermometer, add 50 grams of cyclohexane, add 3.8 grams of zinc chloride and 39 grams of dicyclohexylamine, and slowly add 13.9 grams of butylene oxide under stirring conditions , reflux at 80°C to 90°C for 9 hours to generate N,N-dihydroxyisopropylcyclohexylamine. After the reaction is completed, the solvent and unreacted substances are distilled off under reduced pressure, and the product is purified by gel chromatography. Elution was performed twice with acetone-ethyl acetate at a volume ratio of 20:30 to obtain N,N-dicyclohexylamine-2-butanol as a colorless liquid.
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