Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formamide | HCID 713 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | Methyl 3-carbamoylisobutyrate | HCID 11768702 | — |
| Produkt | Formamide | HCID 713 | — |
| Produkt | Butanedioic acid, 2-methyl-, 1,4-dimethyl ester | HCID 15350 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05618953 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-f419fd2893ef45fb8f0259106ff5352c |
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| Quellennotiz | uspto-grants-1997_04 |
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