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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742018생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/742018

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxybenzenesulfonyl chlorideHCID 7401—
반응물TriethylamineHCID 8471—
반응물D-ValineHCID 71563—
반응물1,4-Dioxane--water (1/1)HCID 21886435—
용매DichloromethaneHCID 6344—
생성물N-[4-methoxybenzenesulfonyl]-(D)-valineHCID 1133588—

반응 단계

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-methoxybenzenesulfonyl 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-methoxybenzenesulfonyl]-(D)-valine t-butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05552419
출처 데이터셋uspto-grants-1996_09
ORD IDord-ffb4a8a670de40a5b54566af8288d822
출처 메모uspto-grants-1996_09