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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58606Erstellt: 24. Oktober 2026

Oxalyl chloride → Ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylate

https://huagongshe.com/de/reaction/58606

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt3-(Trifluoromethyl)benzeneacetic acidHCID 67695—
EduktDiisopropylethylamineHCID 81531—
EduktEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylateHCID 668321614%

Reaktionsschritte

This compound was prepared according to general method 2 with (step I) 2-(3-(trifluoromethyl)phenyl)acetic acid (0.773 g; 3.78 mmol) and oxalyl chloride (0.352 mL; 4.16 mmol) in dichloromethane (12 mL) with few drops of DMF and (step II) ethyl 2-amino-2-(hydroxyimino)acetate (0.5 g; 3.78 mmol) and N,N diisopropylethylamine (1.05 mL; 6.06 mmol) in dichloromethane (6 mL) and (step III) pyridine (18 mL). The crude material was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.040 g (4%) of ethyl 5-(3-(trifluoromethyl)benzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434722B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-b52d720bc7124155aa8989ca832bdea6
Quellennotizuspto-grants-2016_09