A kind of synthetic method of n,n-dicyclohexylamine-2-butanol
A technology of dicyclohexylamine and dicyclohexylamine, which is applied in chemical instruments and methods, preparation of amino hydroxyl compounds, preparation of organic compounds, etc., can solve problems such as limited application coverage and few product varieties, and achieve improved anode electrode Chemical performance, corrosion inhibition effect
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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 reaction at 80℃~85℃ for 8 hours to generate N,N-dicyclohexylamine-2-butanol. After the reaction is completed, the solvent and unreacted substances are distilled off under reduced pressure, and the product is purified by gel chromatography , and eluted three times with acetone-ethyl acetate with a volume ratio of 20:30 to obtain colorless liquid N,N-dicyclohexylamine-2-butanol.
Embodiment 2
[0014] In a four-neck 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 reaction at 85℃~90℃ for 7 hours to generate N,N-dicyclohexylamine-2-butanol. After the reaction is completed, the solvent and unreacted substances are distilled off under reduced pressure, and the product is purified by gel chromatography , and eluted three times with acetone-ethyl acetate with a volume ratio of 20:30 to obtain colorless liquid N,N-dicyclohexylamine-2-butanol.
Embodiment 3
[0016] In a four-neck 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 reaction at 80℃~90℃ for 9 hours to generate N,N-dicyclohexylamine-2-butanol. After the reaction is completed, the solvent and unreacted substances are distilled off under reduced pressure, and the product is purified by gel chromatography , and eluted twice with acetone-ethyl acetate at a volume ratio of 20:30 to obtain colorless liquid N,N-dicyclohexylamine-2-butanol.
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