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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049727Generated: November 4, 2026

Formaldehyde → HCID 20343477, compound

https://huagongshe.com/reaction/2049727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTolueneHCID 1140—
ReactantSodium hydrideHCID 24758—
ReactantPhenol, 4-[(dimethylamino)methyl]-2,6-bis(1,1-dimethylethyl)-HCID 66609—
ReactantHCID 20343467HCID 20343467—
ReactantBis(1,2,2,6,6-pentamethylpiperidin-4-yl) propanedioateHCID 20343478—
ProductHCID 20343477HCID 20343477—

Reaction Steps

21.9 g (0.05 mole) of ethylmalonic acid-bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)ester, 20.5 g (0.05 mole) of malonic acid-bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)ester, 1.5 g (0.05 mole) of paraformaldehyde and 0.5 g of NaH are stirred in 120 ml of toluene for half an hour at room temperature and then for 7 hours at reflux temperature. After cooling, there is added 13.2 g (0.05 mole) of N-(3,5-di-tert.butyl-4-hydroxybenzyl)-dimethylamine, and the mixture is heated for 4 hours under reflux. Processing analogously to Example 1 yields 1-(3,5-di-tert.butyl-4-hydroxyphenyl)-2,2,4,4-tetra-(1,2,2,6,6-pentamethyl-4-piperidinyloxycarbonyl)-hexane as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198334
Source datasetuspto-grants-1980_04
ORD IDord-79536e3b95fb44b097ab290b107767e1
Source noteuspto-grants-1980_04