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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 82815Erstellt: 25. Oktober 2026

Nitrogen → (E)-(2-Styryloxazol-4-yl)methanol

https://huagongshe.com/reaction/82815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktPotassium Sodium TartrateHCID 9357—
EduktDiisobutylaluminum hydrideHCID 14487—
Eduktethyl 2-[(E)-2-phenylethenyl]-1,3-oxazole-4-carboxylateHCID 5708074—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(E)-(2-Styryloxazol-4-yl)methanolHCID 13657827—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (E)-ethyl 2-styryloxazole-4-carboxylate (WO 2009077990 A1) (8.5 g, 34.9 mmol) in THF (28.3 mL) was treated dropwise at 0° C. with DiBAL-H (85.0 mL of a 1.0 M solution in toluene, 85.0 mmol) and the resulting solution was stirred for 1.5 h at 0° C. Rochelle's salt solution was added followed by EA and the mixture was stirred for 24 h at rt. The aq. layer was extracted with EA (3×40 mL) and the combined org. layers were dried over Na2SO4, filtered and the solvent was removed under reduced pressure to give the title compound as an orange oil. TLC: rf (1:1 hept-EA)=0.20. LC-MS-conditions 07: tR=0.71 min, [M+H]+=202.15.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846733B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-d289919e7d224af9845e4292dcbe03d5
Quellennotizuspto-grants-2014_09