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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22969생성일: 2026년 10월 24일

Hydrochloric Acid → 4-[(2-{(2R)-2-[(1E,3S)-3-hydroxyoct-1-enyl]-5-oxopyrrolidin-1-yl}ethyl)thio]butanoic acid methyl ester

https://huagongshe.com/ko/reaction/22969

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
반응물methyl 4-[(2-{(5R)-2-oxo-5-[(1E)-3-oxooct-1-enyl] pyrrolidin-1-yl}ethyl)thio]-butanoateHCID 12132851—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물4-[(2-{(2R)-2-[(1E,3S)-3-hydroxyoct-1-enyl]-5-oxopyrrolidin-1-yl}ethyl)thio]butanoic acid methyl esterHCID 1213285229.6%

반응 조건

온도-30 °C

반응 단계

A solution of methyl 4-[(2-{(5R)-2-oxo-5-[(1E)-3-oxooct-1-enyl]pyrrolidin-1-yl}ethyl)thio]-butanoate (0.039 g, 0.1 mmol) in 2 mL of anhydrous toluene was added dropwise to a −30° C. solution of (R)-2-methyl-CBS-oxazaborolidine (1 M in toluene, 0.05 mL, 0.05 mmol) and borane-methyl sulfide complex (10 M, 0.01 mL, 0.1 mmol). The reaction was stirred for 7 hours at −30° C. and then a solution of hydrochloric acid in methanol (2 M, 1-2 mL) was added. The solution was warmed to room temperature and the solvents were removed via reduced pressure. The crude residue was purified via chromatography yielding 11 mg of 4-[(2-{(2R)-2-[(1E,3S)-3-hydroxyoct-1-enyl]-5-oxopyrrolidin-1-yl}ethyl)thio]butanoic acid methyl ester as an oil. This was taken directly on to the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849657B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-8aa5e02b8b4542b18d3d5fa4e489be9c
출처 메모uspto-grants-2005_02