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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398531Generated: October 31, 2026

Water → N-(3,5-Di-tert-butyl-4-hydroxyphenyl)benzamide

https://huagongshe.com/reaction/2398531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium HydroxideHCID 14798—
Reactant4-Amino-2,6-di-tert-butylphenolHCID 314220—
SolventAcetoneHCID 180—
ProductN-(3,5-Di-tert-butyl-4-hydroxyphenyl)benzamideHCID 1256185890.6%

Reaction Steps

11.05 g (0.05 mole) 2,6-di-t-butyl-4-aminophenol is dissolved in 25 ml acetone and 7.03 g (0.05 mole) benzoyl chloride is added thereto. The reaction is exothermic. The mixture is shaken and 10 ml of 5 N sodium hydroxide is added thereto, portionwise, accompanied by agitation. A solid material separates and is allowed to stand for one hour, cooled and there is then added thereto 50 ml water. The mixture is filtered, washed with 50 ml water and then four times each time with 50 ml portions of petroleum ether to remove the red color. The solid material is air dried and there is obtained 14.72 g (a yield of 90.6%) of the 4-benzamido-2,6-di-t-butylphenol product. The solid material is dissolved in 100 ml of 90% ethanol, contacted with a charcoal adsorbent (Darco G-60) and then crystallized. The crystalline material is cooled, filtered, washed with 30 ml cold 90% ethanol and then dried in vacuo over phosphorus pentoxide. The pure product is characterized by a melting point of 209°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025487
Source datasetuspto-grants-1977_05
ORD IDord-f94c07a1afa649989b622be9ac2d00dc
Source noteuspto-grants-1977_05