HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → alpha-chloro-alpha-(2,4-dichlorophenyl)-acetic acid-N-2-butyl-N-methyl amide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | N-Methyl-2-butanamine | HCID 111026 | — |
| Edukt | alpha-Chloro-alpha-(2,4-dichlorophenyl)-acetyl chloride | HCID 20564372 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | alpha-chloro-alpha-(2,4-dichlorophenyl)-acetic acid-N-2-butyl-N-methyl amide | HCID 20564362 | 64,2% |
Reaktionsschritte
While stirring, 15.2 g of N-2-butyl-N-methylamine is dripped into a solution of 22.4 g of α-chloro-α-(2,4-dichlorophenyl)-acetyl chloride (see a)) in 100 ml of dioxane. After the exothermic reaction has subsided, the mixture is stirred overnight and then poured into 700 ml of ice water; the resultant mixture is acidified with dilute hydrochloric acid and the oil which has precipitated is extracted 8 times, each time with 100 ml of dichloromethane. The extracts are combined, dried over magnesium sulfate and concentrated; there is obtained 17.2 g of α-chloro-α-(2,4-dichlorophenyl)-acetic acid-N-2-butyl-N-methyl amide as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04297364 |
| Quelldatensatz | uspto-grants-1981_10 |
| ORD ID | ord-4cd6978016b644e3867acf9699e09439 |
| Quellennotiz | uspto-grants-1981_10 |