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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499725생성일: 2026년 10월 27일

Cyclohexane → 3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-(2,5-bis(trityloxymethyl)phenyl)tetrahydropyran-2-ol

https://huagongshe.com/reaction/499725

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexaneHCID 8078—
반응물3,4,5-Tribenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-oneHCID 4585508—
반응물2-Bromo-1,4-bis(trityloxymethyl)benzeneHCID 68458085—
반응물CID 53628100HCID 178418400—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-(2,5-bis(trityloxymethyl)phenyl)tetrahydropyran-2-olHCID 7808890880.1%

반응 단계

Under a nitrogen stream, to a solution of 2-bromo-1,4-bis(trityloxymethyl)benzene (255.3 mg, 0.36 mmol) in toluene (1.5 ml), a cyclohexane solution of sec-butyllithium (0.99 M, 367 μl, 0.36 mmol) was added dropwise at room temperature and the solution was stirred for 30 minutes. This solution was added dropwise at −78° C. to a solution of 3,4,5-trisbenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-one (140 mg, 0.26 mmol) in toluene (1.5 ml) and the mixture was stirred at the same temperature for 30 minutes. After addition of water, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then evaporated under reduced pressure to remove the solvent. The resulting residue was purified by silica gel column chromatography (developing solution=ethyl acetate:n-hexane (1:5)) to give the titled compound (242 mg, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767651B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-4fb96350c384456ebcf449f9b89690e7
출처 메모uspto-grants-2010_08