HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium Iodide → N-[(4-Chlorophenyl)methyl]-N-(5-phenylthiophen-2-yl)benzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | N-(5-Phenyl-2-thienyl)-benzamide | HCID 23341604 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[(4-Chlorophenyl)methyl]-N-(5-phenylthiophen-2-yl)benzamide | HCID 23341615 | 51,2% |
Reaktionsschritte
The amide of Example 53 (2.8 g, 0.01 mole) in dimethylformamide (25 ml.) was added to sodium hydride (0.0105 mole) (from 40-50% NaH in oil, 0.74 g) which was stirred in dimethylformamide (25 ml.) and cooled in ice. The mixture was stirred for 0.5 hr. and treated with a solution of p-chlorobenzyl chloride (3.22 g, 0.02 mole) in DMF (15 ml.) and a trace of NaI. The mixture was stirred, initially at ice-bath temperature and them at room temperature overnight and then refluxed for 3 hours to complete the reaction. The DMF was evaporated off, water was added, the product extracted with chloroform, which was dried (Na2SO4), filtered and evaporated to give the N-p-chlorobenzyl-benzamide (2.07 g.) as a viscous oil, b.p. 240°-245° C./0.35 mm.Hg.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04222946 |
| Quelldatensatz | uspto-grants-1980_09 |
| ORD ID | ord-addf2b9ec90943a3879b3d89bdf657d3 |
| Quellennotiz | uspto-grants-1980_09 |