참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Trimethylsilyl triflate | HCID 65367 | — |
| 반응물 | 1-[(Benzoyloxy)methoxymethyl]thymine | HCID 14843535 | — |
| 반응물 | Pentan-3-yl dihydrogen phosphate | HCID 54112757 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 1-[(Diethylphosphonomethoxy)methoxymethyl]thymine | HCID 14886532 | — |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05726174 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-32e98db4036848ce8b8264c0ec0c3131 |
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| 출처 메모 | uspto-grants-1998_03 |
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