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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339284Generated: October 26, 2026

Styrene → Isobutylene styrene

https://huagongshe.com/reaction/339284

Reaction equation

Participants

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

Reaction Conditions

Temperature-70 °C

Reaction Steps

In a 2 L reaction vessel equipped with a stirrer, 589 mL of methylcyclohexane (dried over molecular sieves), 613 mL of n-butyl chloride (dried over molecular sieves) and 0.550 g of cumyl chloride were charged. After cooling the reaction vessel to −70° C., 0.35 mL of a-picoline (2-methylpyridine) and 179 mL of isobutylene were added. Further, 9.4 mL of titanium tetrachloride was added to start polymerization, and then the solution was reacted for 2.0 hours while being stirred at −70° C. Next, 59 mL of styrene was added into the reaction vessel and the reaction was continued for 60 minutes, and then the reaction was terminated by adding a large amount of methanol. After removing the solvent and the like from the reaction solution, a polymer was dissolved in toluene and washed twice with water. This toluene solution was added to the methanol mixture, thereby precipitating a polymer, and the resultant polymer was dried at 60° C. for 24 hours to obtain a styrene-isobutylene diblock copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08893756B2
Source datasetuspto-grants-2014_11
ORD IDord-d5f2995ff3554ab88448916b8364c38c
Source noteuspto-grants-2014_11