HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → Ethyl N-butyl-N-(4-methyl-2-oxazolyl)-carbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | 2-Oxazolamine, N-butyl-4-methyl- | HCID 12295226 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Ethyl N-butyl-N-(4-methyl-2-oxazolyl)-carbamate | HCID 23468959 | — |
Reaktionsschritte
Ethyl chloroformate (10.5 ml, 0.11 mol) was added dropwise over 20 minutes to a stirred solution of 2-butylamino-4-methyl oxazole (15.4 g, 0.10 mol) and triethylamine (15.3 ml, 0.11 mol) in dry ether (100 ml) cooling to 5°-10° C. The mixture was stirred for a further 2 hours at ambient temperature, the white solid was filtered off and the filtrate evaporated under vacuum to a pale oil (22.4 g) NMR (CCl4) 6.3 δ (oxazole 5-H). This 3-acylated compound was dissolved in xylene and the solution was heated under reflux for 2 hours, cooled, washed with dilute HCl, saturated NaCl solution, dilute Na2CO3 and NaCl solution again, dried and evaporated. The residue was distilled under vacuum, b.p. 85°-90° C./0.6 mm NMR (CCl4) 7.12 δ (oxazole 5-H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04175131 |
| Quelldatensatz | uspto-grants-1979_11 |
| ORD ID | ord-709efc0ae90d46f48803521f1b89afcb |
| Quellennotiz | uspto-grants-1979_11 |