HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzene → N-(4-fluoro-alpha,alpha-dimethylbenzyl)-o-methylphenylacetamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzene | HCID 241 | — |
| Edukt | o-Tolyl-acetyl chloride | HCID 2760632 | — |
| Edukt | 1-(4-Fluorophenyl)-1-methylethylamine | HCID 13025665 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N-(4-fluoro-alpha,alpha-dimethylbenzyl)-o-methylphenylacetamide | HCID 12790296 | 78,8% |
Reaktionsschritte
Into a 300 ml four-necked flask, there were charged benzene (200 ml), 4-fluoro-α,α-dimethylbenzylamine (7.7 g) and triethylamine (6.0 g), and o-methylphenylacetyl chloride (9.5 g) was dropwise added thereto at room temperature while stirring, followed by refluxing for 3 hours. After cooling, the reaction mixture was washed with water to remove triethylamine hydrochloride. After the benzene layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol to give 11.3 g of N-(4-fluoro-α,α-dimethylbenzyl)-o-methylphenylacetamide (Compound No. 11). M.P., 150°-151° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04484942 |
| Quelldatensatz | uspto-grants-1984_11 |
| ORD ID | ord-18fc235c6aba47319e43615affca2fd3 |
| Quellennotiz | uspto-grants-1984_11 |