HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Trifluoroacetylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl trifluoroacetate | HCID 9794 | — |
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Trifluoroacetylfuran | HCID 18936315 | — |
Reaction Steps
3-Bromofuran (20 g) was added to a solution of n-butyllithium (2.5M in hexanes, 60 ml) in diethyl ether (200 ml) at -70° C. After 30 minutes, ethyl trifluoroacetate (28.6 g) was added slowly. After a further 1 hour the mixture was allowed to warm to room temperature and was then left to stir overnight. 1M Hydrochloric acid (100 ml) was added and the mixture stirred for 5 minutes. The organic layer was separated, washed, dried and evaporated. The residue was distilled to give the title compound. B.p. 118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05731335 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-ca2c656728094237986dc15e1b9e16c6 |
| Source note | uspto-grants-1998_03 |