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HRID 1464221作成日:2026年10月25日

Water → N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester

https://huagongshe.com/reaction/1464221

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium AcetateHCID 517045—
反応物(S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamateHCID 11128682—
反応物L-phenylalanine methyl ester sulfateHCID 20841682—
溶媒Acetic AcidHCID 176—
生成物N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl esterHCID 1015963073.1%

反応手順

In 100.4 g of acetic acid, 25.1 g (0.1 mole) of N-benzyloxycarbonyl-L-aspartic anhydride was suspended and 22.7 g (0.1 mole) of L-phenylalanine methyl ester sulfate was added with stirring at 5°-10° C. Successively 17.6 g (0.21 mole) of sodium acetate was added at the same temperature. The reaction was carried out for 4 hours with stirring at the same temperature. Thereafter 87.1 g of water was added to the reaction mixture to adjust the concentration of organic carboxylic acid to 53.5% by weight. After cooling to 0°-5° C., precipitated crystals were filtered, washed and dried. Crystals of N-benzyloxycarbonyl-α-L-aspartyl-L-phenylalanine methyl ester were obtained. The yield was 31.2 g (73.1% yield on L-phenylalanine methyl ester sulfate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05302743
出典データセットuspto-grants-1994_04
ORD IDord-a893da5500e64c718ebcd50755c54d72
出典メモuspto-grants-1994_04