摘要
在超声波催化条件下,麦芽酚与苄基氯、胺反应快速地合成了1,2-二甲基-3-羟基-4-吡啶酮和1-乙基-2-甲基-3-羟基-4-吡啶酮,目标产物经IR,1HNMR光谱表征,并与常规合成方法进行了比较,证明该方法使反应时间缩短,产率提高。
1,2-dimethyl-3-hydroxy-4-pyridinone and 1-ethyl-2-methyl-3-hydroxy-4-pyridinone were synthesized from 3-hydroxy-2-methyl-4-pyranone (maltol) and benzyl chloride through three steps of reactions under ultrasonic irradiation. 2-methyl-3-benzyloxy-4-pyranone (1),N-substituted-2-alkyl-3-benzyloxy-4-pyranone (2a,2b),N-substituted-2-alkyl-3-hydroxy-4-pyranone (3a,3b) were synthesized with moderate to high yields (40%~91.55%). The results show that comparing with the conventional thermal reaction,ultrasonic irradiation reaction enjoys very good activities for synthesizing pyridinone compounds. The target compounds were characterized by IR,1H NMR spectra.
出处
《科技导报》
CAS
CSCD
2008年第3期44-45,共2页
Science & Technology Review
基金
全军“十五”指令性课题(3401040-OIL061)
关键词
羟基吡啶酮
超声波催化
合成
hydroxypyridinone
ultrasonic catalysis
synthesis