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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61450생성일: 2026년 10월 24일

Water → 1-benzyl 4-methyl (2S)-2-[benzyl((2R)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinate

https://huagongshe.com/ko/reaction/61450

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium FluorideHCID 5235—
반응물Glycidyl tosylate, (R)-HCID 154187—
반응물TrimethylaluminumHCID 16682925—
반응물Acetone cardiceHCID 18522661—
반응물(S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl esterHCID 67303755—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물1-benzyl 4-methyl (2S)-2-[benzyl((2R)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinateHCID 8734861084.5%

반응 조건

온도-78 °C

반응 단계

To a solution of (2R)-oxiran-2-ylmethyl 4-methylbenzenesulfonate (23.0 g, 0.101 mol) in 500 mL of methylene chloride was added 2.000 M of trimethylaluminum in Toluene (50.4 mL) at −78 Celsius, under an atmosphere of nitrogen. After stirred at −78 Celsius for 10 min, to the mixture was added a solution of (S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl ester (30.0 g, 0.0916 mol) in 150 mL of methylene chloride. The resulting reaction mixture was stirred at −78 Celsius for 30 min. The dry ice-acetone bath was changed to an ice-water bath to warm the mixture up to 0 Celsius. The mixture was stirred at 0 Celsius for 30 min. To the reaction mixture was added sodium fluoride (16.2 g, 0.385 mol) followed by Water (10.4 mL, 0.577 mol) at 0 Celsius. The resulting suspension was rapidly stirred for 1 h at 0 Celsius and filtered through a short column of of Celite and the column was subsequently washed with 600 mL of methylene chloride. The combined filtrates were dried over sodium sulfate, concentrated to dry and purified by column purification (eluting with 0 to 30% EtOAc in hexane) to give The titled compound (43.0 g, 84.4%). MS (ESI): (M+H)+=556.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440958B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-fdb6898bcb9f4dc19e7dcbcf352c1e31
출처 메모uspto-grants-2016_09