Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889478Generated: October 30, 2026

Acetone → Diethyl 1,4-bis(propyloxy)-2,3-naphthalenedicarboxylate

https://huagongshe.com/reaction/889478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant1-BromopropaneHCID 7840—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Diethyl 1,4-dihydroxy-2,3-naphthalenedicarboxylateHCID 43109—
SolventTolueneHCID 1140—
ProductDiethyl 1,4-bis(propyloxy)-2,3-naphthalenedicarboxylateHCID 58017588—

Reaction Conditions

Temperature60 °C

Reaction Steps

Diethyl 1,4-dihydroxy-2,3-naphthalenedicarboxylate* (11 g, 36.1 mmol) was dissolved in acetone (180 ml) and potassium carbonate (24.9 g, 180.5 mmol) added and stirred. 1-Bromopropane (13.1 ml, 144.4 mmol) was added and the reaction mixture was heated at reflux (60° C.) overnight under argon. The reaction was cooled to room temperature and the inorganic solid filtered off. The solvent was evaporated to give an orange brown oil. The residue was taken up in toluene and washed with 5% potassium hydroxide solution, brine and dried over magnesium sulphate. Solvent was removed under vacuum to give a brown oil which was purified by chromatography on silica gel eluting with, 10% ethyl acetate in hexane. The clean fractions were evaporated to give the title compound as yellow oil (11.45 g, 29.5 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252833B2
Source datasetuspto-grants-2012_08
ORD IDord-c7515423828d435997a20d59a2e8f12c
Source noteuspto-grants-2012_08