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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845476Generated: October 30, 2026

6-[2-Imidazol-1-yl-1-(4-methoxy-benzyloxymethyl)-ethoxy]-hexanoic acid ethyl ester → ethyl 6-[2-hydroxy-1-(1H-imidazol-1-yl methyl)ethoxy]hexanoate

https://huagongshe.com/reaction/845476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[2-Imidazol-1-yl-1-(4-methoxy-benzyloxymethyl)-ethoxy]-hexanoic acid ethyl esterHCID 13904806—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTrifluoroacetic acidHCID 6422—
Productethyl 6-[2-hydroxy-1-(1H-imidazol-1-yl methyl)ethoxy]hexanoateHCID 20131189—

Reaction Steps

A solution of ethyl 6-[2-(1H-imidazol-1-yl)-1-[[(4-methoxyphenyl)methoxy]methyl]ethoxy]hexanoate (Example 4; 5.8 g 0.014 mol) in ethanol (20 ml) and trifluoroacetic acid (1 ml) containing a catalytic amount of 10% palladium on carbon (0.5 g) was stirred at room temperature under a hydrogen atmosphere. When hydrogen uptake had ceased the solution was filtered and the solvent was evaporated off under reduced pressure. The residue was treated with a saturated aqueous solution of sodium hydrogen carbonate and extracted with dichloromethane. The extracts were dried (Na2SO4) and the solvent was evaporated off under reduced pressure to give the crude product which was purified by column chromatography (silica gel, chloroform to 5% ethanol in chloroform) to give ethyl

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758573
Source datasetuspto-grants-1988_07
ORD IDord-d929d3f76d6643e3800611245bbb8d47
Source noteuspto-grants-1988_07