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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442073Generated: October 30, 2026

Dibromomethane → 3,3'-Methylene-bis[5-(3",5"-di-tert.-butyl-4"-hydroxy-phenylethyl)-5-methyl-hydantoin]

https://huagongshe.com/reaction/442073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantDimethylformamideHCID 6228—
ReactantPotassium HydroxideHCID 14797—
Reactant5-(3'5'-Di-tert-butyl-4'-hydroxyphenylethyl)-5-methylhydantoinHCID 21416276—
Product3,3'-Methylene-bis[5-(3",5"-di-tert.-butyl-4"-hydroxy-phenylethyl)-5-methyl-hydantoin]HCID 22757770—

Reaction Steps

34.6 g (0.1 mol) of 5-(3',5'-di-tert.-butyl-4'-hydroxyphenylethyl)-5-methyl-hydantoin, 8.7 g (0.05 mol) of methylene bromide and 38 g (0.1 mol) of potassium hydroxide are initially introduced into 100 ml of dimethylformamide and the mixture is kept at 80° C for 16 hours, whilst stirring. After cooling, insoluble matter is filtered off, first 100 ml of toluene and then 100 ml of water are added and the toluene phase is separated off and repeatedly washed with water. Thereafter, 50 ml of toluene are distilled off under reduced pressure and the residual brown solution is left to stand for 24 hours at room temperature. The resulting precipitate is filtered off and recrystallised from acetonitrile.3,3'-methylene-bis[5-(3",5"-di-tert.-butyl-4"-hydroxy-phenylethyl)-5-methyl-hydantoin] of melting point 222° C (stabiliser No. 20) are thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04044019
Source datasetuspto-grants-1977_08
ORD IDord-7f74c83de95a4e9aa29ddaf48f229127
Source noteuspto-grants-1977_08