Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1379221생성일: 2026년 10월 26일
Acetaldehyde → Methyl 3-carboxy-3-(2-ethylidene-1-methylhydrazino)-propionate triethylamine salt
https://huagongshe.com/reaction/1379221
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetaldehyde | HCID 177 | — |
| 반응물 | Methylhydrazine | HCID 6061 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Monomethyl maleate | HCID 5354456 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl 3-carboxy-3-(2-ethylidene-1-methylhydrazino)-propionate triethylamine salt | HCID 86751281 | — |
반응 단계
A solution of 88.5 g methylhydrazine (1.92 moles) in 340 ml THF is added at +25° C. to a solution of 250 g maleic acid monomethyl ester (1.92 moles) and 194.5 g triethylamine (1.92 moles) in 1850 ml THF. During the addition a precipitation of the triethylamine salt of the intermediate methyl 3-carboxy-3-(1-methyl-hydrazino)-propionate is formed. After stirring for 2 hours at +25° C., a solution of 101.6 g acetaldehyde (2.3 moles) in 370 ml THF is added at +25° C. The precipitation dissolves during the addition. After stirring for 1 hour at +25° C. the solution is evaporated completely. To remove traces of water or methanol, the residue is mixed with 750 ml toluene and evaporated again completely (10 mbar, 60° C.). Yield: 429.6 g of methyl 3-carboxy-3-(2-ethylidene-1-methylhydrazine)-propionate triethylamine salt as viscous yellow oil (83%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05670648 |
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| 출처 데이터셋 | uspto-grants-1997_09 |
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| ORD ID | ord-279630d299214a238c1364dceb47b59d |
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| 출처 메모 | uspto-grants-1997_09 |
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