Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,1-Diethoxyethene → 7,7-Diethoxy-3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-triene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,1-Diethoxyethene | HCID 137673 | — |
| 반응물 | 4,5-Dibromoveratrole | HCID 2758033 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 7,7-Diethoxy-3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-triene | HCID 117636365 | 31% |
반응 단계
2.55 g of 1,2-dibromo-4,5-dimethoxybenzene (8.62 mmol; 2 eq) and 500 mg of 1,1-diethoxyethene (4.31 mmol; 1 eq) in 25 mL of toluene are stirred at 0° C. under argon. 3.5 mL of n-butyllithium (2.5M in hexane, 8.62 mmol; 2 eq) are added dropwise at 0° C. When the addition is complete, the reaction mixture is stirred for 22 hours at ambient temperature. The reaction mixture is then hydrolysed and extracted 3 times with ethyl acetate. The organic phases are dried and evaporated, and the crude product is purified by column chromatography over silica gel (eluant: heptane/ethyl acetate 90/10). There are obtained 333 mg of a yellow oil which crystallises at ambient temperature.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08859763B1 |
| 출처 데이터셋 | uspto-grants-2014_10 |
| ORD ID | ord-155f72b8fd384fbb829cf894c0ec540f |
| 출처 메모 | uspto-grants-2014_10 |