Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613270Generated: October 25, 2026

Pyridine → N-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-chlorovaleramide

https://huagongshe.com/reaction/1613270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-Chlorovaleryl chlorideHCID 74089—
Reactant4-Amino-2,6-di-tert-butylphenolHCID 314220—
SolventDiethyl EtherHCID 3283—
ProductN-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-chlorovaleramideHCID 19775707100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of 3.6 g (16 mmol) of 3,5 -di-tert-butyl-4-hydroxyaniline and 1.3 g (16 mmol) of pyridine in 50 ml of ether cooled to 0° C. there was slowly added 2.5 g (16 mmol) of 5-chlorovalerylchloride. The reaction mixture was allowed to warm to 25° C. and stirred for 15 hours following which the mixture was diluted with 100 ml of ether, washed with water, dried over anhydrous magnesium sulfate and concentrated to 5.8 g of solid. The solid was triturated in hexane and filtered to yield 5.5 g (16 mmol) of N-(3,5-di-tert-butyl-4-hydroxyphenyl)-5-chlorovaleramide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192791
Source datasetuspto-grants-1993_03
ORD IDord-6f4d1da7bfd34a369dc6596a9d6b035e
Source noteuspto-grants-1993_03