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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247944Generated: October 31, 2026

Glycerol → 1,6-Naphthyridine

https://huagongshe.com/reaction/2247944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycerolHCID 753—
ReactantSulfuric AcidHCID 1118—
Reactant4-AminopyridineHCID 1727—
ReactantNitrobenzeneHCID 7416—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Product1,6-NaphthyridineHCID 6748818%

Reaction Steps

Glycerol (138.15 g, 1.5 mol) was added dropwise to an ice-cold mixture of "sulfo-mix" (a mixture of nitrobenzene and fuming sulfuric acid, see: Utermohlen, W. P., J. Org. Chem, 1943 8, 544). Addition of 4-aminopyridine (56.46 g, 0.6 mol) was followed by a rapid dropwise addition of water (225 ml), which caused a rise in temperature to 80°; the reaction mixture was allowed to stir until it became homogeneous, and was subsequently heated to 135° for 48 hours. It was then allowed to cool, poured into 1 l ice water, and the pH was adjusted to 13 by the addition of sodium hydroxide pellets. The resulting thick precipitate was removed by filtration, and the filtrate was extracted with methylene chloride (2×2 l). The combined organic extracts were dried over sodium sulfate, filtered, and concentrated to yield a crude product, which was purified by column chromatography (98:2 methylene chloride:methanol). The title product was obtained as an amber oil which crystallized upon standing (13.7 g, 0.11 mol, 18% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037834
Source datasetuspto-grants-1991_08
ORD IDord-a5d21c452de2448bb77c82976e7bfcb3
Source noteuspto-grants-1991_08