HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-[2-(2,6-Dichloroanilino)phenyl]-N,N-dimethylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dichloroaniline | HCID 11846 | — |
| Reactant | 2-(2-Bromophenyl)-N,N-dimethylacetamide | HCID 12884229 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-[2-(2,6-Dichloroanilino)phenyl]-N,N-dimethylacetamide | HCID 12884230 | — |
Reaction Steps
In 80 ml of xylene (having a boiling point of 138° to 141° C.), 8.5 g (0.0525 mole) of 2,6-dichloroaniline was refluxed together with 5.2 g (0.0215 mole) of N,N-dimethyl-o-bromophenylacetamide, 5.0 g (0.0357 mole) of potassium carbonate, 1.0 g of copper powder, 1.0 g of cuprous iodide and 2.0 g of sodium iodide for 48 hours under agitation, while water formed by the reaction was being separated. After completion of the reaction, the reaction mixture was treated with active carbon while it was still warm, and the filtrate was concentrated. The obtained residue was mixed with methyl alcohol and the crystal precipitated on cooling was recovered by filtration, washed with methyl alcohol and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04283532 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-fe076e463aa04bd58d29430088968f09 |
| Source note | uspto-grants-1981_08 |