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HRID 35713作成日:2026年10月23日

Triethylamine → N-t-butoxycarbonyl-L-alanyl-D-alanine benzyl ester

https://huagongshe.com/ja/reaction/35713

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Tert-butoxycarbonylalanineHCID 85082—
反応物D-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)HCID 2802425—
溶媒DichloromethaneHCID 6344—
生成物N-t-butoxycarbonyl-L-alanyl-D-alanine benzyl esterHCID 13369188—

反応手順

To a solution of 23.0 g. (0.121 m) of N-t-butoxycarbonyl-L-alanine, 42.6 g. (0.121 m) of D-alanine benzyl ester p-toluenesulfonic acid salt and 17 ml. (0.121 m) of triethylamine in 400 ml. of cold (0° C.) methylene chloride was added dropwise 25.0 g. (0.121 m) of dicyclohexylcarbodiimide in 100 ml. of methylene chloride. After stirring overnight at room temperature the solids were filtered and the filtrate concentrated to an oil. The residue was dissolved in 400 ml. of ethyl acetate which was washed with a 1% hydrochloric acid solution, a 10% potassium carbonate solution, water and a brine solution. The organic phase was separated, dried over magnesium sulfate and concentrated to an oil. The residue was triturated with diethyl ether and the resulting solids filtered under nitrogen, 16.0 g. An additional 12.7 g. of the desired product crystallized from the filtrate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767743
出典データセットuspto-grants-1988_08
ORD IDord-8a2f92c2d143402187baa2f3871614ad
出典メモuspto-grants-1988_08