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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774243Generated: October 25, 2026

Styrene → Isobutylene styrene

https://huagongshe.com/reaction/1774243

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

Methylcyclohexane (dried with molecular sieves) of 589 mL, n-butyl chloride (dried with molecular sieves) of 613 mL, and cumyl chloride of 0.550 g were added to a 2 L reaction container having an agitator. After cooling the reaction container to −70° C., α-picoline (2-methylpyridine) of 0.35 mL and isobutylene of 179 mL were added. Titanium tetrachloride of 9.4 mL was further added, and the polymerization was stared. The solution was agitated at −70° C. and allowed to react for 2.0 hours. Next, styrene of 59 mL was added to the reaction container, and the reaction was continued for 60 minutes. After that, a large amount of methanol was added to stop the reaction. After a solvent and the like were removed from the reaction solution, the polymer was dissolved in toluene and washed twice. The toluene solution was added to a methanol mixture to deposit the polymer, and the obtained 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 numberUS09259969B2
Source datasetuspto-grants-2016_02
ORD IDord-87527eaccbca4443b490e5c7bedd1d20
Source noteuspto-grants-2016_02