HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1-Methoxy-4-(pentafluoroethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Propanoic acid, 2,2,3,3,3-pentafluoro-, potassium salt (1:1) | HCID 23667659 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | 1-Methoxy-4-(pentafluoroethyl)benzene | HCID 12871966 | — |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
8.3 g of potassium pentafluoropropionate and 9.8 g of CuI are introduced into a 500 ml three-necked flask equipped with Dean-Stark apparatus and a condenser, under an inert atmosphere. 90 ml of DMF and 110 ml of toluene are added. The medium is heated to 140° C. under nitrogen and 80 ml of toluene are distilled off. The medium is then cooled to RT and then deoxygenated by sparging with nitrogen. 6 g of iodoanisole are then added, followed by heating at 155° C. for 20 hours. After cooling to RT, the medium is diluted with 200 ml of a water/ethyl ether mixture. The medium is then filtered through Celite®. The organic phase is washed 3 times with water, dried over MgSO4 and then evaporated to give 4.3 g of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504511B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-fe3059a5e2924c2891b8309964868356 |
| Source note | uspto-grants-2009_03 |