Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434024Generated: October 25, 2026

3-Hydroxy-1-naphthoic acid → 4-Amino-3-hydroxynaphthalene-1-carboxylic acid

https://huagongshe.com/reaction/434024

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxy-1-naphthoic acidHCID 190232—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium sulfanilateHCID 23664644—
ReactantSodium BisulfiteHCID 23665763—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product4-Amino-3-hydroxynaphthalene-1-carboxylic acidHCID 1875643315%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of p-benzenediazonium sulfonate, which was prepared by the addition of sodium sulfanilate (0.525 g, 2.7 mmole) to sodium nitrite at 0°, and the compound from example 14 c) (0.413 g, 2.2 mmol) in water (20 mL), sodium bicarbonate (2.3 g, 27.0 mmol) was added slowly. The resulting solution was heated at 60° C. with stirring overnight. After the solution was cooled to 50° C., sodium hydrogen sulfite (1.05 g, 6.0 mmole) was added. The resulting solution was stirred for 30 min. at 50° C. After cooling down to room temperature, the solid was removed by filtration. The filtrate was evaporated to dryness and the residue was purified by flash chromatography (silica gel, 45% dichloromethane/45% ethyl acetate/10% methanol) to give the title compound (0.066 g, 15%) MS(ES) m/z 203.8 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670387B1
Source datasetuspto-grants-2003_12
ORD IDord-ec1c764de9924c6192c403951b9f64e1
Source noteuspto-grants-2003_12