首页> 外国专利> SHORT TOTAL SYNTHESIS OF DIHYDROTHEBAINONE, DIHYDROCODEINONE AND NORDIHYDROCODEINONE

SHORT TOTAL SYNTHESIS OF DIHYDROTHEBAINONE, DIHYDROCODEINONE AND NORDIHYDROCODEINONE

机译:全合成二氢蒽酮,双氢可待因酮和去甲双氢可待因酮

摘要

ABSTRACT OF THE DISCLOSUREA method of producing morphinan compounds whichincorporates double advantages over the prior art, suchas the utilization of .beta.,.gamma.-unsaturated ketones in placeof the .alpha.,.beta.-unsaturated ketones previously used. Additionally,in the step where .beta.,.gamma.-unsaturated bromoketones proceedto 1-bromo-N-formylnordihydrothebainone (morphinan) thereare utilized super acids, such as trifluoromethane sul-fonic, trifluoroethane sulfonic and mixtures thereof, andalso antimony pentafluoride and mixtures of hydrogenfluoride and antimony pentafluoride. Super acids work,whereas the prior art shows that cyclization in the pres-ence of acids, even strong acids, such as sulfuric, phos-phoric, do not work.
机译:披露摘要一种吗啡喃化合物的制备方法,其与现有技术相比具有双重优势,例如就是利用了β,γ-不饱和酮以前使用的α,β-不饱和酮。另外,在进行β,γ-不饱和溴代酮的步骤中那里的1-溴-N-甲酰基去甲二氢茶黄酮(吗啡喃)用于超强酸,例如三氟甲烷硫磺fonic,三氟乙烷磺酸及其混合物,以及还有五氟化锑和氢的混合物氟化物和五氟化锑。超级酸能起作用而现有技术表明,环化在酸,甚至是强酸,例如硫酸,磷隐喻,不起作用。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号