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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287715Generated: October 26, 2026

4-Methoxyphenol → 4-(p-Methoxyphenoxy)-3-nitro-5-sulphamyl-benzoic acid

https://huagongshe.com/reaction/1287715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
Reactant4-Chloro-3-nitro-5-sulphamoylbenzoic acidHCID 89893—
SolventSodium BicarbonateHCID 516892—
Product4-(p-Methoxyphenoxy)-3-nitro-5-sulphamyl-benzoic acidHCID 21312098—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-chloro-3-nitro-5-sulphamyl-benzoic acid (14 g), p-methoxyphenol (9.3 g), and 1N sodium bicarbonate (200 ml) was stirred at 90° C for 5 hours. After cooling, the resulting 4-(p-methoxyphenoxy)-3-nitro-5-sulphamyl-benzoic acid was precipitated by the addition of 4N hydrochloric acid until the pH was 1, and collected by suction. The crude acid was dissolved in hot methanol (100 ml) and precipitated by the addition of water (100 ml) and cooling. After collection and drying in vacuo, the melting point was 229°-230° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985777
Source datasetuspto-grants-1976_10
ORD IDord-294a22f097ca4feca4a3074e07fddf4f
Source noteuspto-grants-1976_10