Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53363Generated: October 25, 2026

Formamide → Formamide

https://huagongshe.com/reaction/53363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantSulfuric AcidHCID 1118—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-carbamoylisobutyrateHCID 11768702—
ProductFormamideHCID 713—
ProductButanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618953
Source datasetuspto-grants-1997_04
ORD IDord-f419fd2893ef45fb8f0259106ff5352c
Source noteuspto-grants-1997_04