Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2',4',6'-Trihydroxyacetophenone → 1-[2,4,6-Trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| 반응물 | 4-Bromo-2-methylbut-1-ene | HCID 549585 | — |
| 용매 | Potassium Hydroxide | HCID 14797 | — |
| 생성물 | 1-[2,4,6-Trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone | HCID 10979627 | 38.7% |
반응 단계
1-(2,4,6-trihydroxyphenyl]ethanone (2.0 mg, 11.9 mmol) was dissolved in a 5% potassium hydroxide aqueous solution (20 mL). After the mixture was cooled below 0° C., isopentenyl bromide (3.6 g, 24 mmol) was slowly added dropwise within 30 min. The reaction mixture was stirred at room temperature for 2 hours, then poured into an ice water and acidified to pH 2. The reaction mixture was extracted with ethyl acetate. The extract was collected and dried over anhydrous sodium sulfate. After removal of the solvent, the residue was purified by silica gel column chromatography (dichloromethane as eluent) to give the desired compound (0.7 g, yield 20%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09090583B2 |
| 출처 데이터셋 | uspto-grants-2015_07 |
| ORD ID | ord-3cb7b15b61034ec69b25282892b2f98a |
| 출처 메모 | uspto-grants-2015_07 |