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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230891생성일: 2026년 10월 27일

Hydrochloric Acid → 2'-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxy)-6'-hydroxyacetophenone

https://huagongshe.com/reaction/230891

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물2',6'-DihydroxyacetophenoneHCID 69687—
반응물alpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
촉매Benzyltributylammonium chlorideHCID 159952—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물2'-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxy)-6'-hydroxyacetophenoneHCID 1055279443.6%

반응 단계

To a mixture of 2′,6′-dihydroxyacetophenone (1 g), potassium carbonate (4.54 g) and benzyltri(n-butyl)ammonium chloride (0.41 g) in chloroform (13 mL) were added water (0.5 mL) and acetobromo-α-D-glucose (2.7 g), and the mixture was stirred at room temperature for 24 hours. The reaction mixture was poured into water, and the mixture was acidified by addition of 2 mol/L hydrochloric acid. The resulting mixture was extracted with ethyl acetate, and the extract was washed with water and brine. The extract was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was treated with methanol, and the precipitated crystals were collected by filtration and dried under reduced pressure to give the title compound (1.38 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566699B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-9d240b3dce7d47339874ef7064ae6587
출처 메모uspto-grants-2009_07