化工社化工社 化学情報印刷レポート · 研究参考用
Imidazole → (Dimethoxyphosphinyl)[[(1,1-dimethylethyl)dimethylsilyl]oxy]acetic acid (4-nitrophenyl)methyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Imidazole | HCID 795 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 反応物 | Acetic acid, (dimethoxyphosphinyl)hydroxy-, (4-nitrophenyl)methyl ester | HCID 10064522 | — |
| 溶媒 | Diethylether ethylacetate | HCID 21584169 | — |
| 生成物 | (Dimethoxyphosphinyl)[[(1,1-dimethylethyl)dimethylsilyl]oxy]acetic acid (4-nitrophenyl)methyl ester | HCID 9932571 | — |
反応手順
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 50% 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05750735 |
| 出典データセット | uspto-grants-1998_05 |
| ORD ID | ord-393c0b151ecb48a3a1be8a0dcbdc35c0 |
| 出典メモ | uspto-grants-1998_05 |