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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

반응식

참여 물질

역할이름HCID투입량
반응물AcetaldehydeHCID 177—
반응물MethylhydrazineHCID 6061—
반응물TriethylamineHCID 8471—
반응물Monomethyl maleateHCID 5354456—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-carboxy-3-(2-ethylidene-1-methylhydrazino)-propionate triethylamine saltHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05670648
출처 데이터셋uspto-grants-1997_09
ORD IDord-279630d299214a238c1364dceb47b59d
출처 메모uspto-grants-1997_09