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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440411Generated: October 26, 2026

Ethanol → 4-(3,5-Di-tertiary-butyl-4-hydroxyanilino)benzoic acid

https://huagongshe.com/reaction/1440411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-l-oneHCID 15294543—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Product4-(3,5-Di-tertiary-butyl-4-hydroxyanilino)benzoic acidHCID 13960406—

Reaction Steps

To a mixture of 200 ml of ethanol and 25.0 g (0.0736 mole) of 2,6-di(tertiary-butyl)-4-(4'-carboxyphenylimino)-2,5-cyclohexadien-1-one and 12 g (0.087 mole) of potassium carbonate warmed on a steam bath was added 1.0 g of palladium on charcoal. The mixture was reduced using a Paar apparatus for 2 hours. The mixture was diluted with 300 ml of water, filtered through celite, and the filtrate acidified with 6N hydrochloric acid. The yellow solid precipitate was collected by filtration to provide 4-[3,5-di(tertiary-butyl)-4-hydroxyanilino]benzoic acid, m.p. 241°-242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498745
Source datasetuspto-grants-1996_03
ORD IDord-b998f01c036441d3858b1e5a62193bc3
Source noteuspto-grants-1996_03