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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578826Generated: November 1, 2026

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

https://huagongshe.com/reaction/1578826

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 numberUS03939175
Source datasetuspto-grants-1976_02
ORD IDord-9ae17de818ae42d795e5e1c820fa41f9
Source noteuspto-grants-1976_02