HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Fluorouracil → Tegafur
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Fluorouracil | HCID 3385 | — |
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tegafur | HCID 5386 | 64% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04256885 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-792d1a0fbdbe4a3ab41848560b2df4d4 |
| Source note | uspto-grants-1981_03 |