참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Chloro-3-methyl-2-butene | HCID 10429 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethanone, 1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]- | HCID 11687311 | 55% |
반응 단계
In 250 ml of anhydrous tetrahydrofuran was dissolved 50.0 g of 2',4',6'-trihydroxyacetophenone, and 123.1 g of anhydrous potassium carbonate was added to the solution and the mixture was stirred at room temperature for 30 minutes. Then, 37.2 g of 1-chloro3-methyl-2-butene was added dropwise to the mixture over a period of 20 minutes and reaction was carried out at room temperature for 24 hours. After the reaction, the reaction mixture was extracted with 2 l of ethyl acetate and the solvent was removed from the ethyl acetate layer by distillation, and the residue was recrystallized from a benzene/petroleum ether mixed solvent to obtain 38.6 g (yield=55.0%) of 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone in the form of a yellow prism.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05106871 |
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| 출처 데이터셋 | uspto-grants-1992_04 |
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| ORD ID | ord-74e2a1ebf3ec4cde92c5887a9a38f149 |
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| 출처 메모 | uspto-grants-1992_04 |
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