Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzeneacetic acid, 3,4-dimethoxy-, methyl ester → alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzeneacetic acid, 3,4-dimethoxy-, methyl ester | HCID 85213 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 2,3-dihydro-6-methoxy-1H-isoindol-5-ol | HCID 10241135 | — |
| 반응물 | (5-Bromopentyl)(1,1-dimethylethyl)dimethyl silane | HCID 19042078 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | alpha-[5-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]pentyl]-3,4-dimethoxybenzeneacetic acid methyl ester | HCID 54212729 | — |
반응 조건
| 온도 | -78 °C |
|---|
반응 단계
To a solution, -78° C. under argon, of 2 38 g of 3,4-dimethoxyphenyl acetic acid methyl ester in 30 ml of tetrahydrofuran is added 12.45 ml of 1.0M sodium hexamethylsidilazide. The solution is stirred at -78° C. for 5 minutes and then warmed to 0° C. for 1 hour. To this solution is added 3.5 g of (5-bromopentyl)(1,1-dimethylethyl)dimethyl silane. The reaction mixture is allowed to warm to room temperature and stirred for 12 hours. The mixture is diluted with diethyl ether and water, the layers are separated and the organic layer is washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: hexane/ethyl acetate,5/1) to give 2.6 g of the desired product as a clear oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05387685 |
| 출처 데이터셋 | uspto-grants-1995_02 |
| ORD ID | ord-278b8b799112408cad48b628991a6464 |
| 출처 메모 | uspto-grants-1995_02 |