HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoroiodobenzene → HCID 57667991, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoroiodobenzene | HCID 9605 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 68962145 | HCID 68962145 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Binap, (A+-)- | HCID 634876 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57667991 | HCID 57667991 | — |
Reaction Steps
To toluene 4.0 mL suspension of methyl 2-amino-4-(phenoxymethyl)benzoate hydrochloride 0.40 g, rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl 8 mg, palladium acetate 3 mg and cesium carbonate 0.89 g was added 1-fluoro-4-iodobenzene 0.47 mL, and it was heated and refluxed under nitrogen atmosphere for 16 hours. After the reaction mixture was cooled to room temperature, insoluble matter was filtrated, and the solvent was removed under reduced pressure. The obtained residue was refined by silica gel column chromatography [eluent; hexane:ethyl acetate=20:1] to give methyl 2-(4-fluoroanilino)-4-(phenoxymethyl)benzoate 0.22 g of pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08327467B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-efe43bdad2e943b2b29b11cbb191db1f |
| Source note | uspto-grants-2012_12 |