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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526312Generated: October 25, 2026

Styrene → Isobutylene styrene

https://huagongshe.com/reaction/526312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyreneHCID 7501—
ReactantMethylcyclohexaneHCID 7962—
Reactant2-MethylpyridineHCID 7975—
ReactantIsobutyleneHCID 8255—
Reactant(1-Chloro-1-methylethyl)benzeneHCID 70281—
CatalystTitanium TetrachlorideHCID 24193—
SolventMethanolHCID 887—
SolventButyl ChlorideHCID 8005—
ProductIsobutylene styreneHCID 44154101—

Reaction Conditions

Temperature-70 °C

Reaction Steps

Into a 2 L reaction container having an agitator, 589 mL of methylcyclohexane (dried with molecular sieves), 613 ml of n-butyl chloride (dried with molecular sieves), and 0.550 g of cumyl chloride were added. The reaction container was cooled to −70° C., and then 0.35 mL of α-picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization. They were reacted with each other for 2.0 hours while stirring the solution at −70° C. Next, 59 mL of styrene was added to the reaction container, and reaction was continued for another 60 minutes. Thereafter, a large amount of methanol was added to stop the reaction. After removing a solvent and the like from the reaction solution, the polymer was dissolved with toluene and rinsed twice. This toluene solution was added to a methanol mixture to precipitate a polymer. The polymer thus obtained was dried at 60° C. for 24 hours, thereby obtaining a styrene-isobutylene diblock copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346227B2
Source datasetuspto-grants-2016_05
ORD IDord-33458a051763415d9db0f0a2940d31aa
Source noteuspto-grants-2016_05