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HRID 53357作成日:2026年10月25日

L-Serine → N-(Benzyloxycarbonyl)-L-serine

https://huagongshe.com/reaction/53357

反応式

関与物質

役割名称HCID仕込み量
反応物L-SerineHCID 5951—
反応物Benzyl chloroformateHCID 10387—
反応物Sodium HydroxideHCID 14798—
溶媒WaterHCID 962—
生成物N-(Benzyloxycarbonyl)-L-serineHCID 100310—

反応条件

温度25 °C

反応手順

L-Serine (20.00 g, 190.3 mmol) was dissolved in water, and aqueous sodium hydroxide was added to adjust the pH of the solution to about 8.5 while maintaining the temperature at about 25° C. Benzyl chloroformate (36.0 g, 211.0 mmol) was added while the pH was maintained between 8.3 and 8.5 by the addition of aqueous sodium hydroxide and the temperature was maintained at about 30° C. The mixture was stirred for about 2 hours. The reaction mixture was extracted with methylene chloride. The phases were separated, and the pH of the aqueous phase was adjusted to about 7 with concentrated hydrochloric acid. The aqueous phase was heated to about 40° C. under low vacuum to remove any residual methylene chloride. Water was added and the aqueous solution was heated to about 60° C. The pH was adjusted to about 2 with concentrated hydrochloric acid while maintaining the temperature at about 60° C. The solution was cooled to about 50° C. while stirring and seed crystals were added. With stirring, cooling was continued to about 0° C. to complete the crystallization. The product was collected and the cake was washed with cold (about 5° C.) water. The product was dried under vacuum at about 40° C. to afford carbobenzyloxy-L-serine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618946
出典データセットuspto-grants-1997_04
ORD IDord-52ea8117c82a48b084a0887ae07c631a
出典メモuspto-grants-1997_04