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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127689Generated: October 30, 2026

5-Fluorouracil → Tegafur

https://huagongshe.com/reaction/127689

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-FluorouracilHCID 3385—
Reactant2,3-DihydrofuranHCID 70934—
SolventMethyl Ethyl KetoneHCID 6569—
ProductTegafurHCID 538656%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256885
Source datasetuspto-grants-1981_03
ORD IDord-50036ab6cce74d63b65354d80ad652f3
Source noteuspto-grants-1981_03