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HRID 127569作成日:2026年10月25日

Triethylamine → N-(3-methyl-2-nitrobenzyl)-L-alanine ethyl ester

https://huagongshe.com/reaction/127569

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物L-Alanine, ethyl ester, hydrochloride (1:1)HCID 2724356—
反応物1-(Chloromethyl)-3-methyl-2-nitrobenzeneHCID 13573563—
溶媒EthanolHCID 702—
生成物N-(3-methyl-2-nitrobenzyl)-L-alanine ethyl esterHCID 53662574—

反応条件

温度60 °C

反応手順

A solution of 120 ml of triethylamine in 200 ml of absolute ethanol was added dropwise over a period of 30 minutes to a solution of 91.8 g of L-alanine ethyl ester hydrochloride in 300 ml of absolute ethanol. The mixture was warmed to 60° C., a clear solution resulting. To this solution was added dropwise within 1 hour a solution of 55.5 g of 3-(chloromethyl)-2-nitrotoluene in 300 ml of absolute ethanol. Thereafter, the temperature was increased to 80° C. and the mixture was stirred at this temperature overnight. Thereafter, the mixture was evaporated to dryness under reduced pressure and the residue was dissolved in 600 ml of water. The solution was extracted three times with methylene chloride and the extracts were washed successively with water and with saturated sodium chloride solution, dried and evaporated. The thus-obtained crude product was purified by chromatography on silica gel using methylene chloride/5% methanol for the elution. There was obtained N-(3-methyl-2-nitrobenzyl)-L-alanine ethyl ester in the form of a yellow oil; [α]D =-36° (c=1% in methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04256748
出典データセットuspto-grants-1981_03
ORD IDord-5e1a7c3b4bd34045881c833d66613aa9
出典メモuspto-grants-1981_03