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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266913Generated: October 28, 2026

Isoamyl Nitrite → HCID 135718531, compound

https://huagongshe.com/reaction/1266913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
Reactant2-NaphtholHCID 8663—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 14676216HCID 14676216—
SolventEthanolHCID 702—
ProductHCID 135718531HCID 135718531—

Reaction Steps

Next, a reaction flask was loaded with the crystals of 2-amino-3-butoxypyridine (4.4 g), ethanol (25 ml), and sodium ethoxide (2.2 g), followed by dropwise addition of isopentyl nitrite (3.8 g) to the flask in 30 minutes with stirring. The resultant mixture was heated and stirred at 75 to 80° C. for four hours for reaction. The heating was stopped, and the reaction mixture was cooled to room temperature, followed by dropwise addition of 2-naphthol (2.6 g) dissolved in ethanol (10 ml) to the mixture in 10 minutes. The resultant mixture was stirred at room temperature for one hour, heated, and stirred at 75 to 80° C. for additional two hours, followed by stopping the heating and then leaving the mixture to stand overnight. The reaction mixture was condensed by an evaporator. The residue was dissolved in ethyl acetate and, after being successively washed with an aqueous solution of sodium hydroxide and water, the ethyl acetate layer was condensed by an evaporator, followed by addition of methanol to the residue for crystallization. The resultant was filtrated and the crystals were dried to give intended crystals (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06551682B1
Source datasetuspto-grants-2003_04
ORD IDord-d8840db37aa04a0faf95d948578a2312
Source noteuspto-grants-2003_04