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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901048Generated: October 30, 2026

O-Phenylenediamine → N-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamide

https://huagongshe.com/reaction/1901048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamideHCID 2337011632.4%

Reaction Steps

To a solution of 3,5-di-t-butyl-4-hydroxybenzoic acid (5.0 g) in methylene chloride (20 ml) was added dicyclohexylcarbodiimide (2.17 g) and the mixture was stirred overnight at room temperature. Subsequently, triethylamine (2.1 ml), 4-dimethylaminopyridine (0.37 g) and o-phenylenediamine (1.08 g) were added and the mixture was stirred overnight at room temperature. The insolubles was filtered off and the filtrate was concentrated to dryness. The residue was purified by a silica gel column chromatography (chloroform:ethyl acetate=20:1) and crystallized from diisopropyl ether to give N-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamide (1.10 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576335
Source datasetuspto-grants-1996_11
ORD IDord-971f76d4d15449d0ab5c868d448dc7b5
Source noteuspto-grants-1996_11