Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Imidazole → (Dimethoxyphosphinyl)[[(1,1-dimethylethyl)dimethylsilyl]oxy]acetic acid (4-nitrophenyl)methyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | Acetic acid, (dimethoxyphosphinyl)hydroxy-, (4-nitrophenyl)methyl ester | HCID 10064522 | — |
| 용매 | Diethylether ethylacetate | HCID 21584169 | — |
| 생성물 | (Dimethoxyphosphinyl)[[(1,1-dimethylethyl)dimethylsilyl]oxy]acetic acid (4-nitrophenyl)methyl ester | HCID 9932571 | — |
반응 단계
To a mixture of 3.48 g of product from Example 97 and 12 ml of dimethylformamide is added 1.86 g of t-butyldimethylsilyl chloride and 1.86 g of imidazole. After stirring the reaction at room temperature for 2 hours, the mixture is diluted with ethyl acetate/diethyl ether, washed 5 times with water, once with saturated sodium bicarbonate and once with saturated sodium chloride. The organic layer is dried, filtered and concentrated in vacuo to give 3.90 g of the desired silylated product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05602118 |
| 출처 데이터셋 | uspto-grants-1997_02 |
| ORD ID | ord-f2ade3ebbf2c4c00a248280dd5841099 |
| 출처 메모 | uspto-grants-1997_02 |