HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → Diethyl (2-nitrophenyl)phosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | o-Iodonitrobenzene | HCID 69115 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl (2-nitrophenyl)phosphonate | HCID 12547206 | — |
Reaction Steps
3.9 g of Cu(II) acetate are added to a solution of 5 g 1-iodo-2-nitrobenzene and 5 g of triethylphosphite in 20 ml of EtOH, the mixture obtained is refluxed for 24 hours, cooled to rt and partitioned between EtOAc and half-saturated aqueous NaCl-solution. The organic layer obtained is dried, solvent is evaporeated and the evaporation residue is subjected to column chromatography (silicagel, toluene:acetonitrile=3:1). (2-Nitro-phenyl)-phosphonic acid diethyl ester is obtained in the form of an orange oil. MS: MNa+ 282
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119617B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-7340998abfa942cb96692f7ad97fe9a8 |
| Source note | uspto-grants-2012_02 |