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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412510Generated: October 25, 2026

Styrene → Styrene-butadiene-styrene

https://huagongshe.com/reaction/412510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyreneHCID 7501—
Reactant1,3-ButadieneHCID 7845—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant2,2'-Methylenebis(4-methyl-6-tert-butylphenol)HCID 8398—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventCyclohexaneHCID 8078—
ProductStyrene-butadiene-styreneHCID 22280236—

Reaction Steps

186 g of butadiene and 2.4 ml of a 0.5 M solution of tetramethylethylenediamine in cyclohexane is introduced into 4 litres of deaerated cyclohexane. After compensation for the impurities supplied by the solvent and the monomer using n-butyllithium, 3.7 ml of a 0.5 mol/l solution of n-butyllithium in cyclohexane is introduced. The polymerization of the polybutadiene block is effected at 60° C. After conversion of all the butadiene, 114 g of styrene is introduced, which is polymerized at 60° C. for 60 minutes. The copolymer is then protonated by addition of a large excess of methanol in solution in toluene, antioxidized by the addition of 2,2′- methylene bis(4-methyl-6-tert. butylphenol) (1 g per 100 g of monomer), then recovered by steam stripping and dried in an oven at reduced pressure at 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562923B1
Source datasetuspto-grants-2003_05
ORD IDord-247349b812b04a4781e5343d11f8e06f
Source noteuspto-grants-2003_05