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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1918596Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1918596

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
EduktDiisopropylethylamineHCID 81531—
Edukt2-[4-(Trifluoromethoxy)phenyl]acetic acidHCID 2777319—
EduktEthyl 2-amino-2-(hydroxyimino)acetateHCID 6785548—
LösungsmittelPyridineHCID 1049—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 5-(4-(trifluoromethoxy)benzyl)-1,2,4-oxadiazole-3-carboxylateHCID 6683217210,4%

Reaktionsschritte

This compound was prepared according to general method 2 with (step I) 2-(4-(trifluoromethoxy)phenyl)acetic acid (0.833 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); (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 0.124 g (10%) of ethyl 5-(4-(trifluoromethoxy)benzyl)-1,2,4-oxadiazole-3-carboxylate as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08618138B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-b3dd6c971bd446f58eb60988143a3cd5
Quellennotizuspto-grants-2013_12