돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330721생성일: 2026년 10월 23일

Water → Styrene-butadiene-styrene

https://huagongshe.com/ko/reaction/330721

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PyridineHCID 1049—
반응물Perfluorooctanoyl chlorideHCID 78978—
용매TetrahydrofuranHCID 8028—
생성물Styrene-butadiene-styreneHCID 22280236—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877428B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-a2afdab8a8ec495d9e96ec32754212be
출처 메모uspto-grants-2014_11