摘要
以丙泊酚为原料,经过三氯化铁氧化、硼氢化钠还原两步反应得到了丙泊酚杂质E,收率73.5%。丙泊酚杂质J是由丙泊酚经氧化剂硝酸铈铵氧化得到,收率78-3%。目标化合物的结构经MS和。HNMR确证。该合成方法简单,原料易得,操作简单,收率较高。
Propofol impurity E was synthesized via oxidation and reduction using propofol as raw material while impurity J was obtained by oxidizing of propofol in the presence of ammonium cerium nitrate; yields were 73.5% and 78.3%, respectively. These two compounds were confirmed by 1H NMR and MS spectra. This synthetic method was simple with easy-obtaining raw materials and high reaction yield.
出处
《精细化工中间体》
CAS
2016年第2期39-40,53,共3页
Fine Chemical Intermediates
关键词
丙泊酚
杂质
合成
propofol
impurity
synthesis