HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254328Generated: October 25, 2026
2,4-Dimethylfuran → 2-[4-(2-Thienyl)butyryl]3,5-dimethylfuran
https://huagongshe.com/reaction/2254328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dimethylfuran | HCID 19462 | — |
| Reactant | Acetic acid, 2,2-dichloro-, 1,1'-anhydride | HCID 77772 | — |
| Reactant | 4-(2-Thienyl)Butyric Acid | HCID 78386 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-[4-(2-Thienyl)butyryl]3,5-dimethylfuran | HCID 19745237 | 90% |
Reaction Steps
In 50 ml of dichloroethane were dissolved 8.51 g (0.05 mole) of 4-(2-thienyl)butyric acid and 14.39 g (0.06 mole) of dichloroacetic anhydride. To the resulting solution was added 0.065 mole of 3,5-dimethylfuran and 0.71 g of boron trifluoride-diethyl ether complex and the resulting mixture was then stirred at 50° C. for 7 hours. After completion of the reaction, the reaction solution was cooled and washed successively with 5% aqueous sodium carbonate solution and water. The organic layer was concentrated under reduced pressure to obtain 2-[4-(2-thienyl)butyryl]3,5-dimethylfuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05235068 |
|---|
| Source dataset | uspto-grants-1993_08 |
|---|
| ORD ID | ord-b193a9e606e44f6099d3fdb5674a580b |
|---|
| Source note | uspto-grants-1993_08 |
|---|