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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2408162Erstellt: 25. Oktober 2026

Styrene → Isobutylene styrene

https://huagongshe.com/reaction/2408162

Reaktionsgleichung

Beteiligte Stoffe

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

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

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 α-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. The resultant styrene-isobutylene diblock copolymer has a weight-average molecular weight of 70,000 and a styrene unit content of 15% by mass.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08815033B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-e6a1c91ed9a94ae08fd5035513497206
Quellennotizuspto-grants-2014_08