Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344792Generated: October 25, 2026

1-(4-(1-Ethoxyethoxy)phenyl)ethyl butyrate → 1-(4-(1-Ethoxyethoxy)phenyl)ethanol

https://huagongshe.com/reaction/344792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-(1-Ethoxyethoxy)phenyl)ethyl butyrateHCID 54484855—
SolventEthanolHCID 702—
SolventPotassium HydroxideHCID 14797—
Product1-(4-(1-Ethoxyethoxy)phenyl)ethanolHCID 5441849990%

Reaction Steps

In 210 ml of 1N ethanol solution of potassium hydroxide was dissolved 28 g (0.1 mole) of the R-form of 1-(4-(1-ethoxyethoxy)phenyl)ethyl butyrate obtained in Example 2 (i), (ii) or (iii), the mixture was reacted at room temperature over night, and the reaction mixture was concentrated under reduced pressure To the residue was added 200 ml of ether, and it was washed with 2N aqueous solution of sodium hydroxide 2 times and then with water 3 times. The resulting ether layer was dried with anhydrous magnesium sulfate and ether was distilled under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane=1/4) to give 18.9 g of R-form of 1-(4-(1-ethoxyethyoxy)phenyl)ethanol (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053507
Source datasetuspto-grants-1991_10
ORD IDord-025c720f50414656a12d46e08c818d85
Source noteuspto-grants-1991_10