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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128403Erstellt: 24. Oktober 2026

Triethylamine → HCID 12883871, Verbindung

https://huagongshe.com/de/reaction/128403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBenzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-HCID 16197—
Edukt2-Chloromethyl-4-(2-methylbenzyl)-1,3,4-oxadiazolin-5-oneHCID 12883869—
LösungsmittelO-XyleneHCID 7237—
ProduktHCID 12883871HCID 1288387148,4%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A solution of 2-chloromethyl-4-(2-methylbenzyl)-1,3,4-oxadiazolin-5-one (13.3 g) in xylene (35 cc) is added in the course of 20 minutes to a solution of 2-(4-chlorophenyl)-3-methyl-butyric acid (19 g) and triethylamine (11.7 cc) in xylene (175 cc) heated to 110° C. The reaction mixture is heated at the reflux temperature for 4 hours and, after cooling, is washed successively with water (100 cc), a 3.5% strength aqueous hydrochloric acid solution (100 cc), a 4% strength aqueous sodium carbonate solution (100 cc) and water (100 cc). After drying, decolorizing over animal charcoal and concentrating under reduced pressure, the residue obtained is purified by chromatography on a silica column and gives [4-(2-methylbenzyl)-1,3,4-oxadiazolin-5-on-2-yl]-methyl 2-(4-chlorophenyl)-3-methylbutyrate (11.2 g) in the form of an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04259497
Quelldatensatzuspto-grants-1981_03
ORD IDord-53442acee1e346a1bf3a4760912d145e
Quellennotizuspto-grants-1981_03