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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262539Generated: October 30, 2026

Nitrogen oxide (N2O4) → 2-Nitro-3-phenylnaphtho-[1,2-b]furan-5-carboxylic acid

https://huagongshe.com/reaction/262539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogen oxide (N2O4)HCID 25352—
Reactant3-Phenylnaphtho-[1,2-b]furan-5-carboxylic acidHCID 15571609—
SolventChloroformHCID 6212—
Product2-Nitro-3-phenylnaphtho-[1,2-b]furan-5-carboxylic acidHCID 15571606—

Reaction Conditions

Temperature20 °C

Reaction Steps

The product of step A is dissolved partially in 125 ml. of hot chloroform, and 1 g. of dinitrogen tetraoxide is added. The mixture is stirred at 20° C. for about one day. The mixture is evaporated to provide a residue which is triturated with isopropyl alcohol. The residue is separated by filtration and recrystallized from acetic acid to provide light yellow crystals of 2-nitro-3-phenylnaphtho-[1,2-b]furan-5-carboxylic acid, m.p. 286°-288° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154848
Source datasetuspto-grants-1979_05
ORD IDord-d3164cda0dfd4b68b8e1f48196148533
Source noteuspto-grants-1979_05