HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
DI-Sec-butylamine → N,N-Di(butan-2-yl)-2,3,5-trichlorobenzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | DI-Sec-butylamine | HCID 12277 | — |
| Edukt | 2,3,5-Trichlorobenzoyl chloride | HCID 13011116 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | N,N-Di(butan-2-yl)-2,3,5-trichlorobenzamide | HCID 21509368 | — |
Reaktionsschritte
Into a 250 ml flask, provided with a reflux condenser, were introduced 10 g of 2,3,5-trichlorobenzoyl chloride in 20 ml of anhydrous C6H6, a solution of 5.3 g of di-sec.butylamine in 7 ml of anhydrous C6H6 and 5 g of triethylamine. This mass was then heated to reflux temperature for about 1 hour. Thereupon it was left to cool down to room temperature and the solvent was removed under reduced pressure in a rotating evaporator. The mass was then washed with acidulated H2O, with H2O and was then extracted with ethyl ether. The etheric extract was then dried on anhydrous Na2SO4, filtered and the solvent removed under reduced pressure. 12.6 g of yellowing crystals of 2,3,5-trichloro-N,N-di-sec.butyl-benzamide were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03982931 |
| Quelldatensatz | uspto-grants-1976_09 |
| ORD ID | ord-2c7964a3b365418f96667e6950372401 |
| Quellennotiz | uspto-grants-1976_09 |