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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 526312Erstellt: 24. Oktober 2026

Styrene → Isobutylene styrene

https://huagongshe.com/de/reaction/526312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStyreneHCID 7501—
EduktMethylcyclohexaneHCID 7962—
Edukt2-MethylpyridineHCID 7975—
EduktIsobutyleneHCID 8255—
Edukt(1-Chloro-1-methylethyl)benzeneHCID 70281—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelMethanolHCID 887—
LösungsmittelButyl ChlorideHCID 8005—
ProduktIsobutylene styreneHCID 44154101—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346227B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-33458a051763415d9db0f0a2940d31aa
Quellennotizuspto-grants-2016_05