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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254881Generated: November 1, 2026

Ethanol → 3-[N-(3,5-di-tertiary-butyl-4-hydroxyphenyl)-4-aminophenyl]propionic acid

https://huagongshe.com/reaction/2254881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-[4-(2,6-Di-tertiary-butylcyclohexadienon-4-ylideneamino)phenyl]propionic acidHCID 22401578—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventHexaneHCID 8058—
Product3-[N-(3,5-di-tertiary-butyl-4-hydroxyphenyl)-4-aminophenyl]propionic acidHCID 1396040277.1%

Reaction Steps

A mixture of 4.0 g of 3-[4-(2,6-di-tertiary-butylcyclohexadienon-4-ylideneamino)phenyl]propionic acid, 200 ml of ethanol of 0.1 g of 10% palladium on charcoal catalyst was placed on a Paar apparatus. Hydrogen uptake was complete after 30 minutes. Under a nitrogen atmosphere, the reaction mixture was filtered to remove catalyst The filtrate was evaporated to give an oil which was coevaporated with hexane to remove all traces of ethanol and then triturated with hexane to give a light orange crystalline solid. This solid was recrystallized from a mixture of ethanol and water to give 3.1 g 3-[N-(3,5-di-tertiary-butyl-4-hydroxyphenyl)-4-aminophenyl]propionic acid, m.p. 140°-142° C. Analysis: Calculated for C23H31NO3 : %C, 74.8; %H. 8.5; %N. 3.8; Found: %C, 74.7; %H, 8.3; %N, 3.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05237070
Source datasetuspto-grants-1993_08
ORD IDord-d130951ae5ee4c21b3a6596512775528
Source noteuspto-grants-1993_08