HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl 2-(trifluoromethyl)furan-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Reactant | (2-Trifluoromethyl-furan-3-yl)-methanol | HCID 17953606 | — |
| Product | Ethyl 2-(trifluoromethyl)furan-3-carboxylate | HCID 4737733 | — |
Reaction Steps
43.g of the product of Stage A were refluxed for 2 and a half hours in 250 ml of toluene and 3.1 g of toluenesulfonic acid and the reaction mixture was allowed to cool and was chromatographed on silica (eluent: 9/1 hexane/ethyl acetate) to obtain after evaporation of the solvent at 40° C. under 80 mm of Hg, 20 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405865 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-11b84bce1d4444bb92259494d505390c |
| Source note | uspto-grants-1995_04 |