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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 584465Erstellt: 25. Oktober 2026

Acetic Acid → ethyl (6E)-6-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-6-phenylhexanoate

https://huagongshe.com/reaction/584465

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium AcetateHCID 517045—
EduktEthyl 6-oxo-6-phenylhexanoateHCID 3681727—
Edukt3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 10924946—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl acetate hexaneHCID 21226206—
Produktethyl (6E)-6-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-6-phenylhexanoateHCID 1104968458,1%

Reaktionsschritte

After a mixture of 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (600 mg), ethyl 6-oxo-6-phenylhexanoate (452 mg), acetic acid (0.331 ml), sodium acetate (317 mg) and ethanol (20 ml) was heated to reflux for 15 hours, the mixture was cooled to room temperature. Water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain ethyl E-6-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-6-phenylhexanoate (590 mg, yield 58%) as a colorless oil from an ethyl acetate-hexane (2:9, v/v)-eluted fraction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06924300B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-de45dab177e14a9aa43543dc7e9cf35b
Quellennotizuspto-grants-2005_08