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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53363생성일: 2026년 10월 23일

Formamide → Formamide

https://huagongshe.com/ko/reaction/53363

반응식

참여 물질

역할이름HCID투입량
반응물FormamideHCID 713—
반응물Sulfuric AcidHCID 1118—
반응물Sodium MethoxideHCID 10942334—
반응물Methyl 3-carbamoylisobutyrateHCID 11768702—
생성물FormamideHCID 713—
생성물Butanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618953
출처 데이터셋uspto-grants-1997_04
ORD IDord-f419fd2893ef45fb8f0259106ff5352c
출처 메모uspto-grants-1997_04