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HRID 53365生成日期:2026年10月23日

甲酸甲酯 → 甲酰胺

https://huagongshe.com/zh-CN/reaction/53365

反应方程式

参与物

角色名称HCID投料
反应物甲酸甲酯HCID 7865—
反应物Methyl 3-carbamoylisobutyrateHCID 11768702—
反应物HCID 178418416HCID 178418416—
溶剂(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮HCID 887—
产物甲酰胺HCID 713—
产物甲基丁二酸二甲酯HCID 15350—

反应步骤

The procedure in Example 3 (3) was repeated to proceed with heating stirring reaction except that in place of 180 g of methyl formate and 96 g of methanol, 200 g of methanol was charged in the autoclave and carbon monoxide was pressurized into the autoclave so as to maintain the internal pressure at 40 kg/cm2G. After the temperature of the content in the autoclave reached 60° C., carbon monoxide was fed in the autoclave so as to maintain the internal pressure at 40 kg/cm2G to proceed with the reaction for 3 hours. Subsequently, the content therein was cooled, internal pressure was gradually lowered to atmospheric pressure, and the reaction product was taken out. As a result of analysis therefor, the conversion of methyl 3-carbamoylisobutyrate was 81.4% and there were obtained dimethyl methylsuccinate at a selectivity of 95.7% and formamide at a selectivity of 94.4%, each based on the reacted methyl 3-carbamoylisobutyrate.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US05618953
来源数据集uspto-grants-1997_04
ORD IDord-e5055da4b54a4b05b2c5db3de2eb6879
来源说明uspto-grants-1997_04