Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46758Erstellt: 24. Oktober 2026

Triethylamine → Ethyl N-butyl-N-(4-methyl-2-oxazolyl)-carbamate

https://huagongshe.com/de/reaction/46758

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
Edukt2-Oxazolamine, N-butyl-4-methyl-HCID 12295226—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl N-butyl-N-(4-methyl-2-oxazolyl)-carbamateHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04175131
Quelldatensatzuspto-grants-1979_11
ORD IDord-709efc0ae90d46f48803521f1b89afcb
Quellennotizuspto-grants-1979_11