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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257618Erstellt: 25. Oktober 2026

Benzoin → HCID 15232721, Verbindung

https://huagongshe.com/reaction/257618

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoinHCID 8400—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktMonomethyl azelateHCID 75009—
EduktAmmonium AcetateHCID 517165—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 15232721HCID 1523272178%

Reaktionsschritte

A mixture of benzoin (6.00 g, 28 mmol), azelaic acid monomethyl ester (7.17 g of 92% pure material, 32 mmol), 1,3-dicyclohexylcarbodiimide (7.00 g, 34 mmol), 4-dimethylaminopyridine (catalytic amount) and dichloromethane (120 mL) was stirred at room temperature. After 16 hours, the mixture was filtered and the solvent evaporated. Ammonium acetate (10.90 g, 141 mmol) and acetic acid (150 mL) were added to the residue and the mixture heated at reflux for 65 minutes before being cooled and diluted with water. The mixture was extracted with diethyl ether, the combined extracts dried over sodium sulfate and concentrated in vacuo. The residual oil was chromatographed on a column of silica gel using a mixture of hexanes and diethyl ether (7:3) as eluent to give methyl 4,5-diphenyl-2-oxazoleoctanoate (8.24 g, 77%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05262540
Quelldatensatzuspto-grants-1993_11
ORD IDord-1e7f1509404b4317bcfb630e66fb2d25
Quellennotizuspto-grants-1993_11