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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257598Generated: October 24, 2026

1-Nitronaphthalene → 4-Nitro-1-naphthylamine

https://huagongshe.com/en/reaction/257598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitronaphthaleneHCID 6849—
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium ChlorideHCID 25517—
SolventDimethyl SulfoxideHCID 679—
Product4-Nitro-1-naphthylamineHCID 13057—

Reaction Steps

3.5 g of 1-nitronaphthalene and 3.3 g of N,N-tetramethylenethiocarbamoylsulphenamide, dissolved in 15 ml of dimethyl sulphoxide, are added dropwise to a vigorously stirred suspension of 6 g of potassium hydroxide in 50 ml of dimethyl sulphoxide, the temperature being kept at 20° to 25° C. When the addition has ended the mixture is stirred for a further 60 minutes, poured into 400 ml of a saturated aqueous ammonium chloride solution and extracted with methylene chloride. After drying and removing the solvent, 4-nitro-1-naphthylamine is obtained with a melting point of 190° to 192° C. The yield is 2.9 g (77%). 1Nitro-2-napthylamine is additionally obtained in a yield of about 2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262539
Source datasetuspto-grants-1993_11
ORD IDord-7974db6dad9b4a9cad76e2dd880c957c
Source noteuspto-grants-1993_11