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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584394Generated: October 25, 2026

Acetic Acid → ethyl (6E)-6-[(4-hydroxyphenyl)methoxyimino]-6-phenylhexanoate

https://huagongshe.com/reaction/584394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium AcetateHCID 517045—
ReactantEthyl 6-oxo-6-phenylhexanoateHCID 3681727—
Reactant4-(Tert-butyldimethylsilyloxy)benzyloxyamineHCID 11821117—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Productethyl (6E)-6-[(4-hydroxyphenyl)methoxyimino]-6-phenylhexanoateHCID 1108956577%

Reaction Steps

A mixture of 4-(tert-butyldimethylsilyloxy) benzyloxyamine (5.31 g), ethyl 6-oxo-6-phenylhexanoate (6.76 g), acetic acid (3.54 ml), sodium acetate (3.38 g) and ethanol (150 ml) was heated to reflux for 18 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 (100 ml), tetrabutylammonium fluoride trihydrate (10.0 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-6-(4-hydroxybenzyloxyimino)-6-phenylhexanoate (5.64 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 numberUS06924300B2
Source datasetuspto-grants-2005_08
ORD IDord-196adbed6fb24b3780daf4c8312ae455
Source noteuspto-grants-2005_08