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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → Styrene-butadiene-styrene

HRID 44121
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HRID 44121 반응식
N1C=[CH:5][CH:4]=[CH:3][CH:2]=1.F[C:8](F)([C:27](F)(F)F)[C:9](F)(F)[C:10](F)(F)[C:11](F)(F)[C:12](F)(F)[C:13](F)(F)[C:14](Cl)=O.O>O1CCCC1>[CH2:27]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH2:2]=[CH:3][CH:4]=[CH2:5].[CH2:27]=[CH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 1049PyridineHCID 78978Perfluorooctanoyl chloride

생성물 1

HCID 22280236Styrene-butadiene-styrene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

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.

후처리

  1. temperatureheated to
  2. temperaturea mild reflux for an additional 24 hours
  3. customimmediately giving a white precipitate
  4. customreprecipitated into water
  5. customTwo additional tetrahydrofuran-water dissolution-precipitation steps

출처 및 근거

ORD 기록
ord-8f975e7614664bb8bfcbe4b8ea4c9b23
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541162B2

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