関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Trimethylsilyl triflate | HCID 65367 | — |
| 反応物 | 1-[(Benzoyloxy)methoxymethyl]thymine | HCID 14843535 | — |
| 反応物 | Pentan-3-yl dihydrogen phosphate | HCID 54112757 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1-[(Diethylphosphonomethoxy)methoxymethyl]thymine | HCID 14886532 | — |
反応手順
To a solution of 1-[(benzoyloxy)methoxymethyl]thymine (2.9 g, 10 mmol) and diethyl phosphonomethanol (1.85 g, 11 mmol) in benzene (180 mL) was added trimethylsilyl trifluoromethanesulfonate (0.05 mL) via a syringe under nitrogen. The solution was heated at 85° C. for 20 min. After cooling to room temperature, ethyl acetate (50 mL) was added and washed with aqueous bicarbonate, brine dried (MgSO4), filtered and concentrated in vacuo. The resultant yellow oil was purified by silica gel column chromatography using CH2Cl2 /5% MeOH as an eluent to give the title compound as a white oil: yield 980 mg (30%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05726174 |
|---|
| 出典データセット | uspto-grants-1998_03 |
|---|
| ORD ID | ord-32e98db4036848ce8b8264c0ec0c3131 |
|---|
| 出典メモ | uspto-grants-1998_03 |
|---|