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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1041938생성일: 2026년 10월 26일

Triethylamine → 1-Chloro-2-(4-ethynyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzene

https://huagongshe.com/reaction/1041938

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TrimethylsilylacetyleneHCID 66111—
반응물Sodium BicarbonateHCID 516892—
반응물1-chloro-4-(beta-D-glucopyranos-1-yl)-2-(4-trifluoromethylsulfonyloxy-benzyl)-benzeneHCID 86600675—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
생성물1-Chloro-2-(4-ethynyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzeneHCID 86600681—

반응 조건

온도90 °C

반응 단계

25 mg of copper iodide, 44 mg of bis-(triphenylphosphine)-palladium dichloride, 0.30 ml triethylamine and finally 0.14 ml of trimethylsilylacetylene are added under argon to a solution of 0.32 g 1-chloro-4-(β-D-glucopyranos-1-yl)-2-[4-(trifluoromethylsulphonyloxy)-benzyl]-benzene in 3 ml of dimethylformamide. The flask is tightly sealed and the mixture is stirred for 8 h at 90° C. Then another 25 mg of bis-(triphenylphosphine)-palladium dichloride and 0.1 ml trimethylsilylacetylene are added, and the solution is stirred for a further 10 h at 90° C. Then aqueous sodium hydrogen carbonate solution is added, the resultant mixture is extracted three times with ethyl acetate, and the combined organic phases are dried over sodium sulfate. After the solvent has been evaporated, the residue is dissolved in 5 ml of methanol and combined with 0.12 g potassium carbonate. The mixture is stirred for 1 h at ambient temperature and then neutralised with 1 M hydrochloric acid. Then the methanol is evaporated off, the residue is combined with brine and extracted with ethyl acetate. The organic extracts collected are dried over sodium sulfate, and the solvent is removed. The residue is purified by chromatography on silica gel (dichloromethane/methanol 1:0->5:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557782B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-1889e3c0912446aeaae81ef778a9ba96
출처 메모uspto-grants-2013_10