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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44121Erstellt: 24. Oktober 2026

Water → Styrene-butadiene-styrene

https://huagongshe.com/de/reaction/44121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPyridineHCID 1049—
EduktPerfluorooctanoyl chlorideHCID 78978—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktStyrene-butadiene-styreneHCID 22280236—

Reaktionsschritte

A solution of 10% hydroxylated SBS copolymer (3.5 g, 4.5 mmol reactive OH group) dissolved in anhydrous tetrahydrofuran (250 mL) was treated first with pyridine (0.72 g, 9.1 mmol) followed by pentadecafluorooctanoyl chloride (2.08 g, 4.81 mmol). The resulting solution was stirred under argon at room temperature for one hour and then heated to a mild reflux for an additional 24 hours. The reaction mixture was poured into water (500 mL), immediately giving a white precipitate. The crude product was redissolved into tetrahydrofuran (200 mL) and then reprecipitated into water. Two additional tetrahydrofuran-water dissolution-precipitation steps were used to obtain the desired product in purified form. The fluoroalkylated copolymer was then dried in vacuo at 40 degrees C. for 48 hours to give a white, elastomeric solid. The product was stored in the dark under an argon atmosphere. Analysis of the product by FTIR revealed the absence of a broad peak centered near 3329 cm−1 consistent with the esterification of the reactive hydroxyl groups within the copolymer's backbone. An additional signal near 1780 cm−1 (ester carbonyl stretch) was also observed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541162B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-8f975e7614664bb8bfcbe4b8ea4c9b23
Quellennotizuspto-grants-2013_09