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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070076Generated: October 25, 2026

Acetic Acid → ethyl (8E)-8-[(4-hydroxyphenyl)methoxyimino]-8-phenyloctanoate

https://huagongshe.com/reaction/1070076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium AcetateHCID 517045—
ReactantEthyl 8-oxo-8-phenyloctanoateHCID 10934282—
Reactant4-(Tert-butyldimethylsilyloxy)benzyloxyamineHCID 11821117—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Productethyl (8E)-8-[(4-hydroxyphenyl)methoxyimino]-8-phenyloctanoateHCID 2234457377%

Reaction Steps

A mixture of 4-(tert-butyldimethylsilyloxy)benzyloxyamine (3.10 g), ethyl 8-oxo-8-phenyloctanoate (6.32 g), acetic acid (2.07 ml), sodium acetate (1.98 g) and ethanol (80 ml) was heated under reflux for 20 hours. The reaction mixture was cooled to room temperature, water was added 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 dissolved in tetrahydrofuran (60 ml), tetrabutylammonium fluoride trihydrate (3.98 g) was added and stirred at room temperature for 1 hour. 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-hydroxybenzyloxyimino)-8-phenyloctanoate (3.55 g, yield 77%) as a colorless oil from an ethyl acetate-hexane (2:7, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-67085f1dc1d04d699cf8a76cf13a89ec
Source noteuspto-grants-2001_06