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HRID 264278作成日:2026年10月26日

4-Methoxybenzenesulfonyl chloride → N-[4-methoxybenzenesulfonyl]-(D)-valine

https://huagongshe.com/reaction/264278

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methoxybenzenesulfonyl chlorideHCID 7401—
反応物TriethylamineHCID 8471—
反応物D-ValineHCID 71563—
反応物1,4-Dioxane--water (1/1)HCID 21886435—
溶媒DichloromethaneHCID 6344—
生成物N-[4-methoxybenzenesulfonyl]-(D)-valineHCID 1133588—

反応手順

To a solution of D-valine (15.0 g, 128.0 mmol) in 1:1 dioxane/water (200 mL) containing triethylamine (19.4 g, 192.0 mmol) at room temperature is added 4-methoxybenzene-sulfonyl chloride (29.0 g, 141.0 mmol), and the reaction mixture is stirred at room temperature overnight. The mixture is then diluted with methylene chloride, washed with 1N aqueous hydrochloric acid and water. The organic layer is washed again with brine, dried (Na2SO4), and the solvent is evaporated to provide N-[4-methoxybenzenesulfonyl]-(D)-valine as a crude product. A solution of this crude product (15.0 g) in toluene (100 mL) containing N,N-dimethylformamide di-t-butyl acetal (50 mL, 206.5 mmol) is heated to 95° C. for 3 hours. The solvent is then evaporated. The crude product is purified by silica gel chromatography (30% ethyl acetate/hexanes) to provide N-[4-methoxybenzene-sulfonyl]-(D)-valine t-butyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646167
出典データセットuspto-grants-1997_07
ORD IDord-94c9da312d5f43789f00688d9c9edd22
出典メモuspto-grants-1997_07