Method for preparing alcohol compounds by amine compounds
A technology for amine compounds and aldehyde compounds, which is applied in the field of preparing alcohol compounds from amine compounds, achieves the effects of simple operation process, reduced energy consumption, and avoidance of strong acid systems
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Embodiment 1
[0035] Add acetophenone (48.00g, 0.40mol) in 500mL there-necked flask, benzaldehyde (21.20g, 0.20mol), isopropylamine (11.80g, 0.20mol) and aluminum chloride (1.40g, 10.00mmol), in The reaction was carried out at 30°C without solvent, followed by TCL. After the reaction was completed, it was filtered, and the filtrate was distilled to obtain the corresponding product isopropanol, which was detected by gas chromatography with a purity of 98% and a yield of 80%.
Embodiment 2
[0037] Add acetophenone (72.00g, 0.60mol) in 500mL there-necked flask, benzaldehyde (21.20g, 0.20mol), n-butylamine (14.60g, 0.20mol) and L-proline trifluoromethanesulfonate ( 2.64g, 10.00mmol), reacted under the reflux condition of ethanol (100.00mL), followed by TCL. After the reaction was completed, the product was filtered, and the filtrate was rectified to obtain the corresponding product n-butanol, which was detected by gas chromatography with a purity of 97% and a yield of 93%.
Embodiment 3
[0039] Add p-methylacetophenone (80.40g, 0.60mol), benzaldehyde (21.20g, 0.20mol), glycine (15.00g, 0.20mol) and diphenylamine trifluoromethanesulfonate (3.20mol) in a 500mL three-necked flask g, 10.00 mmol), reacted at 150°C under solvent-free conditions, and followed the reaction with TCL. After the reaction was completed, the product was filtered, and the filtrate was distilled to obtain the product 2-hydroxyacetic acid, which was detected by gas chromatography with a purity of 93% and a yield of 90%.
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