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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 972699Erstellt: 25. Oktober 2026

Benzene → Styrene t-butylstyrene

https://huagongshe.com/reaction/972699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktStyreneHCID 7501—
Edukttert-ButylstyreneHCID 138033—
EduktButyllithiumHCID 178418339—
LösungsmittelMethanolHCID 887—
LösungsmittelHeptaneHCID 8900—
ProduktStyrene t-butylstyreneHCID 86733069—

Reaktionsschritte

Under anaerobic and anhydrous conditions 400 ml of purified benzene is charged to a polymerization vessel followed by 0.53 milliequivalents of n-butyllithium in heptane. t-Butylstyrene (9.0 g, 0.056 mole) is added at about 30° C., and the resultant solution is stirred 15-30 minutes at 30°-60° C. Six more monomer additions are made as follows: styrene (18.0 g, 0.173 mole), t-butylstyrene (9.0 g), styrene (18.0 g), t-butylstyrene (9.0 g), styrene (18.0 g), and t-butylstyrene (9.0 g). Between additions the solution is permitted to stir for 15-30 minutes at 30°-60° C. The polymerization solution is then inactivated by the addition of a small quantity of methanol, and the seven block copolymer is isolated by precipitation with methanol in a Waring blender. The precipitated block copolymer is thoroughly washed with methanol and vacuum oven dried at 80° C. for 24 hours. A quantitative yield (90 g) of block copolymer is obtained. Gel permeation chromatography shows the copolymer to possess a narrow molecular weight distribution. A molded film of the block copolymer is clear and transparent. The calculated degree of polymerization of the seven block copolymer is 1400, and the calculated molecular weight is 170,000.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04053548
Quelldatensatzuspto-grants-1977_10
ORD IDord-1c4081fab95e46e08c43e4fbcf144d41
Quellennotizuspto-grants-1977_10