反応 #214871
ord-50036ab6cce74d63b65354d80ad652f3
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他the mixture was reacted in an autoclave for 2 hours at 180° C
- 2その他After completion of the reaction
- 3その他the reaction liquid
- 4workup.ADDITIONwas treated in the same manner
- 5その他was recovered as a substance insoluble in chloroform
実験手順
Into 30 ml of methyl ethyl ketone were suspended 1.3 g of 5-fluorouracil. To this suspension were added 1.4 g of 2,3-dihydrofuran and the mixture was reacted in an autoclave for 2 hours at 180° C. After completion of the reaction, the reaction liquid was treated in the same manner as described in Example 1 whereby 0.38 g of the starting 5-fluorouracil was recovered as a substance insoluble in chloroform and 1.12 g of 1-(2-tetrahydrofuryl)-5-fluorouracil were obtained. The yield of the end product was 79% based on the consumed 5-fluorouracil.