Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963958생성일: 2026년 10월 27일
Hydrochloric Acid → 2'-(beta-D-glucopyranosyloxy)-6'-hydroxy-3-(5-benzo[b]furanyl)acrylophenone
https://huagongshe.com/reaction/963958
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 1-Benzofuran-5-carbaldehyde | HCID 2773875 | — |
| 반응물 | 2'-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxy)-6'-hydroxyacetophenone | HCID 10552794 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2'-(beta-D-glucopyranosyloxy)-6'-hydroxy-3-(5-benzo[b]furanyl)acrylophenone | HCID 67566248 | — |
반응 단계
To a mixture of 2'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-6'-hydroxyacetophenone (965 mg), benzo[b]furan-5-carbaldehyde (350 mg) and ethanol (10 ml) is added dropwise a 50% aqueous potassium hydroxide solution (2 ml), and the mixture is stirred at room temperature overnight. The mixture is evaporated to remove the solvent under reduced pressure, and to the residue are added water and diisopropyl ether. The mixture is stirred, and the aqueous layer is obtained by separation. The aqueous layer is neutralized by using a 10% hydrochloric acid under ice-cooling, and extracted with ethyl acetate. The resulting organic layer is washed with water, dried, and evaporated to remove the solvent to give crude 2'-(β-D-glucopyranosyloxy)-6'-hydroxy-3-(5-benzo[b]furanyl)acrylophenone.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05767094 |
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| 출처 데이터셋 | uspto-grants-1998_06 |
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| ORD ID | ord-40ae2288bea94fd09cf08c3d65ccf2f5 |
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| 출처 메모 | uspto-grants-1998_06 |
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