関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Iodide Ion | HCID 30165 | — |
| 反応物 | Neryl chloride | HCID 5874259 | — |
| 反応物 | HCID 178473686 | HCID 178473686 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | HCID 178473683 | HCID 178473683 | — |
反応手順
To a stirred mixture of 123 mg (5.13 mmol) of sodium hydride in 10 mL of DMF at 0° C. under argon was added 1.32 g (5.13 mmol) of Example 1, Part A [(ethoxymethylphosphinyl)methyl]phosphonic acid, diethyl ester in 5 mL of DMF dropwise over 20 minutes. The mixture was stirred for 0.5 hours and was treated with 1.00 g (3.42 mmol) of Part A iodide in 3 mL of DMF. The reaction was stirred at 0° C. for 1 hour then at room temperature for 48 hours, at which time the reaction was diluted with ether and quenched with saturated NH4Cl. The organic layer was washed with water, brine, dried (MgSO4) and evaporated to provide 1.10 g of a pale yellow oil. Flash chromatography was performed on 100 g of silica gel eluted with 49.5:49.5:1 acetone/ethyl acetate/methanol (1 liter) followed by 45:45:10 acetone/ethyl acetate/methanol. Pure product fractions were combined and evaporated to provide 600 mg (43%) of title ester as a pale yellow oil, a mixture of diastereomers.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05428028 |
|---|
| 出典データセット | uspto-grants-1995_06 |
|---|
| ORD ID | ord-6a90e7ab0f284dfc9b059e1e2c7eb2d0 |
|---|
| 出典メモ | uspto-grants-1995_06 |
|---|