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HRID 1459113作成日:2026年10月23日

Hydrochloric Acid → 2,4-Bis-(4-hydroxybenzyl)-3-azaglutaric acid-diisopropyl ester

https://huagongshe.com/ja/reaction/1459113

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-Hydroxyphenylpyruvic AcidHCID 979—
反応物L-TyrosineHCID 6057—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物2,4-Bis-(4-hydroxybenzyl)-3-azaglutaric acid-diisopropyl esterHCID 54124893—

反応条件

温度60 °C

反応手順

9.01 g (50.0 mmol) of 4-hydroxyphenylpyruvic acid and 9.06 g (50.0 mmol) of tyrosine are dissolved in 60 ml of methanol and stirred for six hours at 60° C. Then, it is allowed to cool to room temperature and 0.76 g (20 mmol) of sodium borohydride is added. It is allowed to stir overnight and then the reaction mixture is mixed carefully with diluted hydrochloric acid until no more gas generation can be observed. The reaction mixture is concentrated by evaporation and dried in an oil pump vacuum for several hours at 100° C. The residue is taken up in isopropanol. Hydrogen chloride gas is introduced until saturation is achieved, stirred for two hours at room temperature and then for eight hours at 85° C. Then, it is concentrated by evaporation, the residue is dispersed between ethyl acetate and sodium bicarbonate solution, the organic phase is dried on sodium sulfate, filtered and concentrated by evaporation. The residue is chromatographed on silica gel with use of hexane/ethyl acetate as mobile solvent. The fractions that contain the pure product are combined and concentrated by evaporation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05853699
出典データセットuspto-grants-1998_12
ORD IDord-7cf6e1c10daa4481929a646a6cf9d50d
出典メモuspto-grants-1998_12