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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Diethyl 1,4-dihydroxy-2,3-naphthalenedicarboxylate | HCID 43109 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl 1,4-bis(propyloxy)-2,3-naphthalenedicarboxylate | HCID 58017588 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252833B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-c7515423828d435997a20d59a2e8f12c |
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| Source note | uspto-grants-2012_08 |
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