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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049725Generated: October 26, 2026

Acetic Acid → Butyl-(3,5-di-tert.butyl-4-hydroxybenzyl)malonic acid-bis(2,3,6-trimethyl-2,6-diethyl-4-piperidinyl) ester

https://huagongshe.com/reaction/2049725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantLithium amideHCID 24532—
ReactantPhenol, 4-[(dimethylamino)methyl]-2,6-bis(1,1-dimethylethyl)-HCID 66609—
ReactantButylmalonic acid-bis(2,3,6-trimethyl-2,6-diethyl-4-piperidinyl)esterHCID 20343463—
SolventTolueneHCID 1140—
ProductButyl-(3,5-di-tert.butyl-4-hydroxybenzyl)malonic acid-bis(2,3,6-trimethyl-2,6-diethyl-4-piperidinyl) esterHCID 20343468—

Reaction Steps

26.2 g (0.05 mole) of butylmalonic acid-bis(2,3,6-trimethyl-2,6-diethyl-4-piperidinyl)ester and 13.2 g (0.05 mole) of N-(3,5-di-tert.butyl-4-hydroxybenzyl) dimethylamine are dissolved in 200 ml of toluene. After the addition of 0.25 g of lithium amide, the mixture is refluxed for 4 hours. After cooling, the mixture is neutralised with 1.5 ml of 1% acetic acid, and the organic phase is repeatedly washed with water. After drying over Na2SO4, the solution is concentrated in vacuo. As residue there is obtained butyl-(3,5-di-tert.butyl-4-hydroxybenzyl)malonic acid-bis(2,3,6-trimethyl-2,6-diethyl-4-piperidinyl) ester in the form of viscous oil (Compound No. 32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198334
Source datasetuspto-grants-1980_04
ORD IDord-19db1396771d4c0ea867166a1302f815
Source noteuspto-grants-1980_04