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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58611Erstellt: 24. Oktober 2026

Water → Ethyl 5-(2,5-dimethoxybenzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/de/reaction/58611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDiisopropylethylamineHCID 81531—
Edukt(2,5-Dimethoxyphenyl)acetyl chlorideHCID 596088—
EduktEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 5-(2,5-dimethoxybenzyl)-1,2,4-oxadiazole-3-carboxylateHCID 6683212437,5%

Reaktionsschritte

2-(2,5-dimethoxyphenyl)acetyl chloride (0.662 mL; 3.78 mmol) was added to a mixture of ethyl 2-amino-2-(hydroxyimino)acetate (0.500 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (18 mL) at −15° C. The reaction mixture was stirred at room temperature overnight and poured into a mixture of ice and water. The formed precipitate was filtered off, suspended in pyridine (18 mL) and refluxed in a sealed tube for 20 h and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.414 g (37%) of ethyl 5-(2,5-dimethoxybenzyl)-1,2,4-oxadiazole-3-carboxylate as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434722B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-afbe7050054a4dcbb592ce5a267bdfc2
Quellennotizuspto-grants-2016_09