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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 264289생성일: 2026년 10월 24일

Dimethylformamide → N-hydroxy-1-[4-methoxybenzenesulfonyl]-pyrrolidine-2(S)-carboxamide

https://huagongshe.com/ko/reaction/264289

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물1-[(4-Methoxyphenyl)sulfonyl]-D-prolineHCID 744902—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N-hydroxy-1-[4-methoxybenzenesulfonyl]-pyrrolidine-2(S)-carboxamideHCID 11022968—

반응 단계

1-[4-Methoxybenzenesulfonyl]-pyrrolidine-2(R)-carboxylic acid (1.12 g, 3.93 mmol) is dissolved in methylene chloride (40.0 mL). To this solution is added oxalyl chloride (0.69 mL, 7.85 mmol) and dimethylformamide (0.30 mL, 3.93 mmol), and the reaction is stirred at room temperature for 30 minutes. Meanwhile, in a separate flask, hydroxylamine hydrochloride (1.1 g, 15.7 mmol) and triethylamine (3.3 mL, 23.5 mmol) are stirred in tetrahydrofuran (20.0 mL) and water (4.0 mL) at 0° C. for 15 minutes. After 30 minutes, the methylene chloride solution is added in one portion to the second flask, and the combined contents are stirred overnight as the flask gradually warms up to room temperature. The reaction is then diluted with acidic water (pH=~3), and extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (50% ethyl acetate/hexane) to give N-hydroxy-1 -[4-methoxybenzenesulfonyl]-pyrrolidine-2(S)-carboxamide, m.p. 163.5°-165.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646167
출처 데이터셋uspto-grants-1997_07
ORD IDord-a4ac08fd061041b2b96b5d4eadf86961
출처 메모uspto-grants-1997_07