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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2',6'-Dihydroxyacetophenone | HCID 69687 | — |
| 반응물 | alpha-D-Glucopyranosyl bromide, tetraacetate | HCID 101776 | — |
| 촉매 | Benzyltributylammonium chloride | HCID 159952 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 2'-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxy)-6'-hydroxyacetophenone | HCID 10552794 | 43.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07566699B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-9d240b3dce7d47339874ef7064ae6587 |
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| 출처 메모 | uspto-grants-2009_07 |
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