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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584472Generated: October 30, 2026

Dimethylformamide → ethyl (8E)-8-[[4-[[2-(furan-2-yl)-5-methyl-1,3-oxazol-4-yl]methoxy]phenyl]methoxyimino]-8-phenyloctanoate

https://huagongshe.com/reaction/584472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl (8E)-8-[(4-hydroxyphenyl)methoxyimino]-8-phenyloctanoateHCID 22344573—
Reactant4-(Chloromethyl)-2-(furan-2-yl)-5-methyl-1,3-oxazoleHCID 22344582—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Productethyl (8E)-8-[[4-[[2-(furan-2-yl)-5-methyl-1,3-oxazol-4-yl]methoxy]phenyl]methoxyimino]-8-phenyloctanoateHCID 2234459984.1%

Reaction Steps

A mixture of 4-(chloromethyl)-2-(2-furyl)-5-methyloxazole (340 mg), ethyl E-8-(4-hydroxybenzyloxyimino)-8-phenyloctanoate (600 mg), potassium carbonate (432 mg) and N,N-dimethylformamide (7 ml) was stirred at room temperature for 18 hours. 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-8-[4-[2-(2-furyl)-5-methyl-4-oxazolylmethoxy]benzyloxyimino]-8-phenyloctanoate (717 mg, yield 84%) 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-bd8b9793e94e4e6a80fbc54090190e93
Source noteuspto-grants-2005_08