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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16723Erstellt: 23. Oktober 2026

Nitrogen → Benzene, ethenyl-, polymer with 1,3-butadiene

https://huagongshe.com/de/reaction/16723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktStyreneHCID 7501—
Edukt1,3-ButadieneHCID 7845—
Edukt1,1-DiphenylethyleneHCID 10740—
EduktTin tetrachlorideHCID 24287—
EduktButyllithiumHCID 178418339—
LösungsmittelHexaneHCID 8058—
ProduktBenzene, ethenyl-, polymer with 1,3-butadieneHCID 62697—

Reaktionsschritte

To a 1-gallon stainless steel reactor under a N2 blanket was charged 3.0 lbs. of 21.5% 1,3-butadiene in technical grade hexane, 3.0 lbs. of technical grade hexane and 67 g of 33% styrene in hexane. All solvents were dried to less than 5 ppm water and oxygen free. 64.7 mmol of nBuLi was charged to the reactor and polymerization was allowed to proceed for 5 and ⅓ hours at 123-127° F. 308 grams of a control sample was taken and live cement was terminated with isopropanol. A second 308 gram sample was also taken. It was calculated that a maximum of 51.3 mmol of carbon-bound lithium was still present in the reactor, 50.4 mmol of 1,1-diphenylethylene and 16 mmol of the vinyl modifier 2,2-di(tetrahydrofuryl)propane were added to the reactor and allowed to react for 2.75 hours at 125° F. and a further 16 hours at ˜70° F. A sample was taken for analysis and it was determined that 23.6% of the 1,1-diphenylethylene remained unreacted. A 306 gram sample was taken in a N2 purged crown-capped bottle and 1.7 mmol SnCl4 were added to terminated and couple the polymer. (It was calculated that a maximum of 0.021 mmol carbon-bound lithium was present per gram of cement.) Both the control sample and the SnCl4 coupled sample were worked up by evaporating the hexane in a rotoevaporator and finishing in a vacuum oven at 50° C. Molecular weight analysis results by Gel Permeation Chromatography (GPC) are shown in Table 3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737218B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4b15a74b8f3b4719813c53862261102f
Quellennotizuspto-grants-2010_06