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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 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 反応物 | Acetic acid, (dimethoxyphosphinyl)hydroxy-, (4-nitrophenyl)methyl ester | HCID 10064522 | — |
| 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 dimethylformide is added 1.86 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 ester, washed 5 times water, once with saturated solid bicarbonate and once with saturated solid 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 | US05623081 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-176add45f66046e7b8a21502c35de5fd |
| 出典メモ | uspto-grants-1997_04 |