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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46186생성일: 2026년 10월 24일

delta-Gluconolactone → (3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-(benzyloxymethyl)-2-(4-chloro-3-((triisopropylsilyloxy)methyl)phenyl)-tetrahydro-2H-pyran-2-ol

https://huagongshe.com/ko/reaction/46186

반응식

참여 물질

역할이름HCID투입량
반응물delta-GluconolactoneHCID 7027—
반응물(5-Bromo-2-chlorobenzyloxy)triisopropylsilaneHCID 67153939—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(3R,4S,5R,6R)-3,4,5-Tris(benzyloxy)-6-(benzyloxymethyl)-2-(4-chloro-3-((triisopropylsilyloxy)methyl)phenyl)-tetrahydro-2H-pyran-2-olHCID 67287055—

반응 단계

To a solution of (5-Bromo-2-chlorobenzyloxy)triisopropylsilane (compound 4, 97 g, 257 mmol) from Step 3 in tetrahydrofuran (1 L) at −78° C. under an atmosphere of nitrogen was added dropwise n-butyllithium (2.5 M in hexanes, 103 mL, 257 mmol), and the mixture was stirred for 1.5 h at the same temperature. Then a solution of 2,3,4,6-tetra-O-benzyl-D-glucopyranone (compound 2, 106 g, 198 mmol) from Step 1 in tetrahydrofuran (500 mL) was added dropwise, and the mixture was stirred for 3 h at the same temperature. The reaction mixture was quenched by addition of saturated ammonium chloride solution. After complete addition, the solution was gradually raised to room temperature. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo to yield the title compound as a yellow oil which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541380B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a780a61119ba441c9529ed88dfc75f77
출처 메모uspto-grants-2013_09