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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487399Generated: October 29, 2026

Diethyl Ether → HCID 19093683, compound

https://huagongshe.com/reaction/487399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 19093751HCID 19093751—
SolventEthanolHCID 702—
ProductHCID 19093683HCID 19093683—

Reaction Steps

Potassium hydroxide (0.112 g) was added to a solution of methyl 4-[(5,7-diethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-1-yl)-methyl]benzoate (A) (0.35 g) in ethanol (10 ml) and the mixture was heated at reflux for 90 minutes. Volatile material was removed by evaporation and the residue was dissolved in a minimum of water which was then acidified with acetic acid. Ether was added to the mixture and the solid which crystallised was collected by filtration. Further solid was obtained by adding petroleum ether to the ether phase of the filtrate. The combined solids were recrystallised from ethyl acetate/petroleum ether to give 4-[(5,7-diethyl-2-oxo-1,2-dihydro-1,6-naphthyridin-1-yl)methyl]benzoic acid (0.175 g), as a solid, m.p. 143°-146° C.; NMR (CDCl3): 1.21(t, 3H), 1.35(t, 3H), 2.79(q, 2H), 3.12(q, 2H), 5.56(s, 2H), 6.77(s, 1H), 6.80(d, 1H), 7.30(d, 2H), 7.81(d, 1H), 8.05(d, 2H); mass spectrum (CI. ammonia): 337 (M+H)+ ; microanalysis, found: C, 71.3; H, 6.3; N, 7.9%; C20H20N2O3 requires: C, 71.4; H, 6.0; N, 8.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294620
Source datasetuspto-grants-1994_03
ORD IDord-5e26232f619a4e978de0650d4dcd2902
Source noteuspto-grants-1994_03