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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584465Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium AcetateHCID 517045—
ReactantEthyl 6-oxo-6-phenylhexanoateHCID 3681727—
Reactant3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 10924946—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Productethyl (6E)-6-[[3-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenyl]methoxyimino]-6-phenylhexanoateHCID 1104968458.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924300B2
Source datasetuspto-grants-2005_08
ORD IDord-de45dab177e14a9aa43543dc7e9cf35b
Source noteuspto-grants-2005_08