The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

以苯乙酸乙酯和乙醇胺为原料合成了苄低毒前体苯乙酰基乙醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基反应引入乙酰基，接着、胺，得到标题树。该法避免了使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

以2-乙酰基苯并咪唑和钠为原料,在光照条件下用氯气置换钠中的,合成兽药噻苯咪唑中间体-2-(二乙酰基)-苯并咪唑氢酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

以苯乙酸乙酯和乙醇胺为原料合成了苄青霉素低毒前体苯乙乙醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付反应引入乙，接着、胺，得到标题树。该法避免了使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

以2-乙苯并咪唑和为原料,在光照条件下用氯气置换出中的素,合成兽药噻苯咪唑中间体-2-(二乙)-苯并咪唑氢酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

苯酸酯和醇胺为原料合成了苄青霉素低毒前体苯酰醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰化反应引入酰，溴化、胺化，得到标题树。该法避免了使用氯甲。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

2-酰苯并咪唑和溴化钠为原料,在光照条件下用氯气置换出溴化钠中的溴素,合成兽药噻苯咪唑中间体-2-(二溴酰)-苯并咪唑氢溴酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

酸酯和醇胺为原料合成了苄青霉素低毒前酰基醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入酰基，接着溴化、胺化，得到标题树。该法避免了使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

2-酰基并咪唑和溴化钠为原料,在光照条件下用氯气置换出溴化钠中的溴素,合成兽药噻咪唑中-2-(溴酰基)-并咪唑氢溴酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

苯酸酯和醇胺为原料合成了苄青霉素低毒前体苯醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏化反应引入，着溴化、胺化，得到标题树。该法避免了使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

2-苯并咪唑和溴化钠为原料,在光照条件下用氯气置换出溴化钠中的溴素,合成兽药噻苯咪唑中间体-2-(二溴)-苯并咪唑氢溴酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

以苯乙酸乙酯和乙醇胺合成了苄青霉素低毒前体苯乙酰基乙醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

氏酰基化反应引入乙酰基，接着溴化、胺化，得到标题树。该法避免了使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

以2-乙酰基苯并咪唑和溴化钠,在光照条件下用氯气置换出溴化钠中的溴素,合成兽药噻苯咪唑中间体-2-(二溴乙酰基)-苯并咪唑氢溴酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

苯乙酸乙酯和乙醇胺为原料合成了苄青霉素低毒前体苯乙酰基乙醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，化、胺化，得到标题树。该法避免了使用氯。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

2-乙酰基苯并咪唑和化钠为原料,在光照条件下用氯气置换出化钠中的素,合成兽药噻苯咪唑中间体-2-(二乙酰基)-苯并咪唑氢酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

以苯乙酸乙酯和乙醇胺为原料苄青霉素低毒前体苯乙酰基乙醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰基化反应引入乙酰基，接着化、胺化，得到标题树。该法避免使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

以2-乙酰基苯并咪唑和化钠为原料,在光照条件下用氯气置换出化钠素,兽药噻苯咪唑间体-2-(二乙酰基)-苯并咪唑氢酸盐。

The phenylacetyl ethanolamine,a low toxic precurson of benzylpenicillin,was synthesized by using ethyl phenylacetate and colamine as raw materials.

以苯乙酸乙酯乙醇胺为原料合成了苄青霉素低毒前体苯乙酰乙醇胺。

The title resin has been prepared by Friedel-Crafts acylation followed by bromination and amination.The method avoids the utilization of cancerogenic chloromethyl methyl ether.

通过付氏酰应引入乙酰，接着、胺，得到标题树。该法避免了使用氯甲醚。

Using 2-acetyl benzimidazole and sodium bromide as raw material,2-(dibromine acetyl)-benzimidazole hydrobromate was synthesized with the new bromine that displaced by chlorine gas in light.

以2-乙酰苯并咪钠为原料,在光照条件下用氯气置换出钠中的素,合成兽药噻苯咪中间体-2-(二乙酰)-苯并咪氢酸盐。