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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53365Generated: October 23, 2026

Methyl formate → Formamide

https://huagongshe.com/en/reaction/53365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantMethyl 3-carbamoylisobutyrateHCID 11768702—
ReactantHCID 178418416HCID 178418416—
SolventMethanolHCID 887—
ProductFormamideHCID 713—
ProductButanedioic acid, 2-methyl-, 1,4-dimethyl esterHCID 15350—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618953
Source datasetuspto-grants-1997_04
ORD IDord-e5055da4b54a4b05b2c5db3de2eb6879
Source noteuspto-grants-1997_04