Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetramethylammonium Hydroxide Pentahydrate → (+/-)-alpha-tert.Butyloxycarbonylamino-3-(4'-chloro-5-(diethoxyphosphinyl)methyl-[1.1'-biphenyl]-3-yl) propanoic acid cinnamyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetramethylammonium Hydroxide Pentahydrate | HCID 82620 | — |
| 반응물 | Bromomethylstyrene | HCID 98116 | — |
| 반응물 | HCID 14127515 | HCID 14127515 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (+/-)-alpha-tert.Butyloxycarbonylamino-3-(4'-chloro-5-(diethoxyphosphinyl)methyl-[1.1'-biphenyl]-3-yl) propanoic acid cinnamyl ester | HCID 56990101 | — |
반응 단계
To a solution of 1.05 g of the product of step b) in 5 ml dimethylformamide are added 362 mg tetramethylammonium hydroxide pentahydrate. The mixture is stirred at room temperature 1 1/2 hours and then treated with 394 mg cinnamyl bromide. The mixture is stirred at room temperature 17 hours. The mixture is diluted with ice/water (about 50 ml) and extracted with diethyl ether. The extracts are washed with 10 ml aqueous 1N KHCO3 solution, dried (Na2SO4) and evaporated to give the heading compound as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05162311 |
| 출처 데이터셋 | uspto-grants-1992_11 |
| ORD ID | ord-01be88585a0243e0b188c3ce031ecad4 |
| 출처 메모 | uspto-grants-1992_11 |