反応 #214870

ord-792d1a0fbdbe4a3ab41848560b2df4d4

反応方程式

O=c1[nH]cc(F)c(=O)[nH]1
5-fluorouracil
C1=COCC1
2,3-dihydrofuran
O=c1[nH]cc(F)c(=O)[nH]1
5-fluorouracil
O=c1[nH]c(=O)n(C2CCCO2)cc1F
1-(2-tetrahydrofuryl)-5-fluorouracil
収率 64.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the mixture was reacted in an autoclave for 5 hours at 170° C
  2. 2
    その他After completion of the reaction
  3. 3
    その他the reaction liquid
  4. 4
    workup.ADDITIONwas treated in the same manner
  5. 5
    その他was recovered as a substance insoluble in chloroform

実験手順

Into 30 ml of tetrahydrofuran 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 5 hours at 170° C. After completion of the reaction, the reaction liquid was treated in the same manner as described in Example 1 whereby 0.30 g of the starting 5-fluorouracil was recovered as a substance insoluble in chloroform and 1.28 g of 1-(2-tetrahydrofuryl)-5-fluorouracil were obtained. The yield of the end product was 83.2% based on the consumed 5-fluorouracil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04256885uspto-grants-1981_03