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HRID 53363生成日期:2026年10月23日

甲酰胺 → 甲酰胺

https://huagongshe.com/zh-CN/reaction/53363

反应方程式

参与物

角色名称HCID投料
反应物甲酰胺HCID 713—
反应物四氧化硫HCID 1118—
反应物甲醇钠HCID 10942334—
反应物Methyl 3-carbamoylisobutyrateHCID 11768702—
产物甲酰胺HCID 713—
产物甲基丁二酸二甲酯HCID 15350—

反应步骤

A one L stainless steel-made autoclave equipped with a stirrer was charged with 72.5 g of the methyl 3-carbamoylisobutyrate which had been obtained in the preceding item (2), 180 g of methyl formate, 96 g of methanol and 1.1 g of sodium methylate to proceed with heating reaction at 60° C. for 2 hours. The reaction product was cooled and then analyzed. As a result, the conversion of the methyl 3-carbamoylisobutyrate was 83.2% and, there were obtained dimethyl methylsuccinate at a selectivity of 99.8% based on the reacted methyl 3-carbamoylisobutyrate, and formamide at a selectivity of 98.4% based on the same. The sodium methylate in the reaction liquid was neutralized with sulfuric acid, and subsequently the reaction liquid was distilled by a conventional method. As a result, methyl formate and methanol were recovered and there were obtained 60 g of dimethyl methylsuccinate with at least 99% purity and 16 g of formamide with 99% purity. The recovery of these substances inclusive of an intermediate fraction was quantitative, respectively.

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-f419fd2893ef45fb8f0259106ff5352c
来源说明uspto-grants-1997_04