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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85709생성일: 2026년 10월 25일

Benzyl Bromide → (2S,3S,4S,5R,6R)-benzyl 3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylate

https://huagongshe.com/reaction/85709

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물TetrahydrofuranHCID 8028—
반응물beta-D-glucopyranuronic acidHCID 441478—
반응물Tetrabutylammonium FluorideHCID 2724141—
용매DimethylformamideHCID 6228—
용매Isopropanol methylene chlorideHCID 21966342—
생성물(2S,3S,4S,5R,6R)-benzyl 3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylateHCID 5814885765%

반응 단계

To a solution of (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxytetrahydro-2H-pyran-2-carboxylic acid (1 g, 5.15 mmol) and TBAF in THF (6.18 mL, 6.18 mmol) in DMF (7 mL) was slowly added (bromomethyl)benzene (0.925 g, 5.41 mmol) at 0° C. The clear solution was warmed up to room temperature slowly and let it stir for 17 hours. TLC indicated the reaction was completed (20% iPrOH/CH2Cl2). The solvent was removed and the reaction residue was purified by silica gel chromatography with 10-20% iPrOH/CH2Cl2 to provide the desired product as a colorless oil (950 mg, 65%). LCMS: m/e 283.31 (M−H)−, 2.55 min (method 10).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846647B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-936e74c96b654b12b1c7a5f7ca94e20b
출처 메모uspto-grants-2014_09