辽宁医学院学报
遼寧醫學院學報
료녕의학원학보
JOURNAL OF LIAONING MEDICAL UNIVERSITY
2015年
3期
7-9
,共3页
吲哚-2-甲酸%1-甲基-3-甲酰基吲哚-2-甲酸甲酯%合成
吲哚-2-甲痠%1-甲基-3-甲酰基吲哚-2-甲痠甲酯%閤成
신타-2-갑산%1-갑기-3-갑선기신타-2-갑산갑지%합성
1H-indole-2-carboxylicacid%methyl3-formyl-1-methyl-1H-indole-2-carboxylate%synthesis
目的:合成1-甲基-3-甲酰基吲哚-2-甲酸甲酯。方法以吲哚-2-甲酸和甲醇为原料经过酯化反应,甲基化和Vilsmeier-haack反应得到标题化合物,总收率为90.3%。结果本方法具有反应条件温和、收率高、易于纯化的特点,为目标化合物的合成提供了新途径。经过核磁共振氢谱和液相-质谱联用对产物进行了结构表征。结论该工艺具有收率高、操作简单、安全可靠的特点并且为工业化生产提供参考。
目的:閤成1-甲基-3-甲酰基吲哚-2-甲痠甲酯。方法以吲哚-2-甲痠和甲醇為原料經過酯化反應,甲基化和Vilsmeier-haack反應得到標題化閤物,總收率為90.3%。結果本方法具有反應條件溫和、收率高、易于純化的特點,為目標化閤物的閤成提供瞭新途徑。經過覈磁共振氫譜和液相-質譜聯用對產物進行瞭結構錶徵。結論該工藝具有收率高、操作簡單、安全可靠的特點併且為工業化生產提供參攷。
목적:합성1-갑기-3-갑선기신타-2-갑산갑지。방법이신타-2-갑산화갑순위원료경과지화반응,갑기화화Vilsmeier-haack반응득도표제화합물,총수솔위90.3%。결과본방법구유반응조건온화、수솔고、역우순화적특점,위목표화합물적합성제공료신도경。경과핵자공진경보화액상-질보련용대산물진행료결구표정。결론해공예구유수솔고、조작간단、안전가고적특점병차위공업화생산제공삼고。
Objective To synthesize methyl 3-formyl-1methyl-1H-indole-2-carboylate. Methods With 1H-indole-2-car-boxylic acid and methanol as starting material, the compound mentioned above was synthesized after esterification as well as reaction of methylation and Vilsmeier-haack, with a total yield of 90. 3%. Results This method boasted the advantages of mild reaction condi-tion, high yield, and easy purification, providing a new way of synthesis of target compound. The structure characterization of the product was completed with 1H-NMR and LC-MS. Conclusion The method has advantages of high yield, simple operation and safe-ty, with reference value for industrialized production. .