関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Fluorouracil | HCID 3385 | — |
| 反応物 | 2,3-Dihydrofuran | HCID 70934 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1,3-Bis(tetrahydro-2-furanyl)-5-fluoro-2,4-pyrimidinedione | HCID 124956 | — |
反応手順
In 20.8 ml of pyridine were dissolved 5.2 g (40 m mol) of 5-fluorouracil and 14 g (200 m mol) of 2,3-dihydrofuran. The solution were heated at about 150° C. in a closed tubular reactor under agitation for 6 hours. After the reaction, the reaction mixture was concentrated to dryness under reduced pressure. The residue was dissolved in chloroform and the solution was passed through a column of silica gel. The column was eluated with chloroform and the effluent was concentrated to dryness under reduced pressure. The residue was washed with a small amount of petroleum ether to give the above-mentioned compound as colorless crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04249006 |
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| 出典データセット | uspto-grants-1981_02 |
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| ORD ID | ord-2992a554a28e4ff7a9ce0121c7aa404d |
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| 出典メモ | uspto-grants-1981_02 |
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