Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl formate → Formamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl formate | HCID 8025 | — |
| 반응물 | Methyl 3-carbamoylisobutyrate | HCID 11768702 | — |
| 생성물 | Formamide | HCID 713 | — |
| 생성물 | Methylsuccinic acid ethyl methyl ester | HCID 54001611 | — |
반응 단계
The procedure in Example 3 (3) was repeated except that ethyl formate was used in place of methyl formate. As a result, the conversion of methyl 3-carbamoylisobutyrate was 83.7% and there were obtained methylsuccinic acid ethyl methyl ester at a selectivity of 99.8% and formamide at a selectivity of 98.6%, each based on the reacted methyl 3-carbamoylisobutyrate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05618953 |
| 출처 데이터셋 | uspto-grants-1997_04 |
| ORD ID | ord-0b2414389f2d435ebd782a575159d2a6 |
| 출처 메모 | uspto-grants-1997_04 |