A kind of synthetic method of β-piperidinyl alcohol
A technology of piperidinyl alcohol and synthesis method, applied in organic chemistry and other directions, can solve the problems of few product varieties and limited application coverage, and achieve the effect of inhibiting corrosion and improving anode polarization performance.
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Embodiment 1
[0013] In a four-necked flask equipped with a stirring device, a reflux condensing device, and a thermometer, add 85 grams of toluene, 9.5 grams of zinc chloride and 34 grams of piperidine, and slowly add 20.9 grams of propylene oxide under stirring conditions, at 90 ° C ~ Reflux reaction at 95°C for 9 hours to generate β-piperidinyl alcohol. After the reaction was completed, the solvent and unreacted substances were distilled off under reduced pressure, and the product was purified by gel chromatographic column, using acetone- Elution was carried out twice with ethyl acetate to obtain β-piperidinyl alcohol as a colorless liquid.
Embodiment 2
[0015] In a four-neck flask equipped with a stirring device, a reflux condensing device, and a thermometer, add 74 grams of toluene, 9 grams of zinc chloride and 37 grams of piperidine, and slowly add 29.8 grams of butylene oxide under stirring conditions, at 95 ° C Reflux reaction at ~100°C for 10 hours to generate β-piperidinyl alcohol. After the reaction was completed, the solvent and unreacted substances were distilled off under reduced pressure, and the product was purified by gel chromatography, using acetone with a volume ratio of 40:60 -Ethyl acetate was eluted twice to obtain β-piperidinyl alcohol as a colorless liquid.
Embodiment 3
[0017] In a four-neck flask equipped with a stirring device, a reflux condensing device, and a thermometer, add 93 grams of toluene, 9.9 grams of zinc chloride and 31 grams of piperidine, and slowly add 21 grams of propylene oxide under stirring conditions, at 90 ° C ~ Reflux reaction at 100°C for 8 hours to generate β-piperidinyl alcohol. After the reaction was completed, the solvent and unreacted substances were distilled off under reduced pressure, and the product was purified by gel chromatography, using acetone- Ethyl acetate was eluted three times to obtain β-piperidinyl alcohol as a colorless liquid.
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