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HRID 437912作成日:2026年10月27日

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

https://huagongshe.com/reaction/437912

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物GlycineHCID 750—
反応物Methyl 3-(chlorocarbonyl)-5-nitrobenzoateHCID 74774—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
生成物N-(3-Methoxycarbonyl-5-nitrobenzoyl)-glycineHCID 21427264—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04032567
出典データセットuspto-grants-1977_06
ORD IDord-8dd9758a60004d5b9cbb359521290246
出典メモuspto-grants-1977_06