A kind of preparation method of n-ethyl-3-phenylpropylamine
A technology for phenylpropylamine and phenylpropanal, applied in the field of compound preparation, can solve the problems of high equipment requirements, violent reaction of reagents, difficult control of use and operation, low requirements for equipment and operators, and avoidance of tertiary amines and quaternary ammonium salt by-products, reducing the effect of environmental impact
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Embodiment 1
[0088] Under nitrogen protection, 20 mmol ethylamine hydrochloride was dissolved in 20 mL methanol, and stirred for 10 min. At -40°C, 20 mmol of 3-phenylpropanal (Formula V) was added dropwise. The progress of the reaction was monitored by gas chromatography. After reaching the end of the reaction, slowly add 5 mmol of NaBH at -40°C 4 , continue to monitor the progress of the reaction by gas chromatography. After reaching the end of the reaction, the temperature was raised to -20°C, and 20 mL of methanol-water (V 甲醇 :V 水 =10:90) solution to quench the reaction, and continue to stir, and monitor the progress of the reaction by gas chromatography. After reaching the end point of the reaction, the reaction was terminated.
Embodiment 2
[0090] Take the reaction solution of Example 1, filter it, evaporate the solvent to dryness under reduced pressure, and adjust the pH=8. The aqueous layer was extracted twice with ethyl acetate, the organic layers were combined, extracted once with water and saturated brine, and the organic layer was collected; dried, filtered, and evaporated to dryness under reduced pressure to obtain the target compound N-ethyl-3-benzene Propylamine (formula I, yield 72%, its purity 85% detected by gas chromatography).
Embodiment 3
[0092] Under the protection of nitrogen, 20 mmol of ethylamine hydrochloride was dissolved in 20 mL of methanol, and after slowly adding 2 mmol of LiOH, the mixture was stirred for 10 min. At -40°C, 20 mmol of 3-phenylpropanal (Formula V) was added dropwise. The progress of the reaction was monitored by gas chromatography. After reaching the end of the reaction, slowly add 5 mmol of NaBH at -40°C 4 , continue to monitor the progress of the reaction by gas chromatography. After reaching the end of the reaction, the temperature was raised to -20°C, and 20 mL of methanol-water (V 甲醇 :V 水 =10:90) solution to quench the reaction, and continue to stir, and monitor the progress of the reaction by gas chromatography. After reaching the end of the reaction, filter, evaporate the solvent under reduced pressure, and adjust the pH to 8. The aqueous layer was extracted twice with ethyl acetate, the organic layers were combined, extracted once with water and saturated brine, and the or...
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