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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 437912생성일: 2026년 10월 26일

Acetone → N-(3-Methoxycarbonyl-5-nitrobenzoyl)-glycine

https://huagongshe.com/reaction/437912

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물GlycineHCID 750—
반응물Methyl 3-(chlorocarbonyl)-5-nitrobenzoateHCID 74774—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
생성물N-(3-Methoxycarbonyl-5-nitrobenzoyl)-glycineHCID 21427264—

반응 단계

Under agitation and during the course of 21/2 hours, 183.0 g. (0.75 mole) of 3-methoxycarbonyl-5-nitrobenzoyl chloride in 750 ml. of acetone is added dropwise to a solution of 62.0 g. (0.825 mole) of glycine and 189.0 G. of sodium bicarbonate in 3 l. of water. The first-obtained precipitate is gradually dissolved again after an additional three hours of agitation. Thereafter, the reaction mixture is extracted twice with ether, the aqueous phase is acidified with concentrated hydrochloric acid, the thus-precipitated oil is extracted repeatedly with ethyl acetate, and the combined ethyl acetate extracts, after washing with water and drying with sodium sulfate, are mixed with a stoichiometric amount of dicyclohexylamine. After allowing the reaction mixture to stand for some time, it is filtered off from the precipitated dicyclohexylammonium salt (m.p. 204°-205° C. form chloroform/ether), washed several times with ether, and the acid is liberated again by distributing the reaction mixture between ethyl acetate and 2 N sulfuric acid. After washing the ethyl phases with water, drying with sodium sulfate, and concentrating under vacuum, 181.0 g. of the above-identified compound is obtained. M.P. 142°-143° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04032567
출처 데이터셋uspto-grants-1977_06
ORD IDord-8dd9758a60004d5b9cbb359521290246
출처 메모uspto-grants-1977_06