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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457592Generated: October 26, 2026

P-Anisidine → 195314-31-9

https://huagongshe.com/reaction/1457592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantButylated HydroxyanisoleHCID 8456—
ReactantSodium HydroxideHCID 14798—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
Product195314-31-9HCID 13571954464.4%

Reaction Steps

p-Anisidine (257 g) was dissolved in 514 ml of conc. hydrochloric acid, and under ice-cooling, 1530 ml of an aqueous solution containing 158 g of sodium nitrite was added dropwise to the solution. This mixture was added dropwise under ice-cooling to 3000 ml of an aqueous solution containing 356 g of 4-methoxy-2-tert-butylphenol and 416 g of sodium hydroxide. The resulting mixture was stirred at the same temperature for 15 minutes. Conc. hydrochloric acid (about 400 ml) was added dropwise to the reaction mixture to adjust pH of the mixture to 3, and the precipitated crystals were collected by filtration. The crystals were washed and dried, and recrystallized from a mixed solution of chloroform and ethanol to give 400 g of 2-(4-methoxyphenylazo)-4-methoxy-6-tert-butylphenol (yield: 64%, melting point: 125°-127° C., IR: 1600 cm-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849732
Source datasetuspto-grants-1998_12
ORD IDord-b437a585c04944d18271f66039854825
Source noteuspto-grants-1998_12