HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2,3,6-Trichlorobenzoic acid → (Aminocarbonyl)Methyl 2,3,6-Trichlorobenzoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2,3,6-Trichlorobenzoic acid | HCID 5759 | — |
| Edukt | Chloroacetamide | HCID 6580 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 18-Crown-6 | HCID 28557 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (Aminocarbonyl)Methyl 2,3,6-Trichlorobenzoate | HCID 2417794 | — |
Reaktionsschritte
This compound was prepared in the manner of Example I, using 15.0 grams (0.066 mole) of 2,3,6-trichlorobenzoic acid, 4.4 grams (0.066 mole) of potassium hydroxide, 6.2 grams (0.066 mole) of 2-chloroacetamide, and 1.8 grams of 1,4,7,10,13,16-hexaoxacyclooctadecane in 300 ml of dry toluene and 200 ml of dimethylformamide. The crude product was purified by liquid chromatography, followed by recrystallization from ethyl acetate. The yield was 0.9 gram of (aminocarbonyl)methyl 2,3,6-trichlorobenzoate; mp 158°-160°. The ir and the nmr spectra were consistent with the proposed structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04309566 |
| Quelldatensatz | uspto-grants-1982_01 |
| ORD ID | ord-f67ddac55063423aa6c6229eb1daa2d8 |
| Quellennotiz | uspto-grants-1982_01 |