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Water → Styrene-butadiene-styrene

HRID 44121
ノート
印刷プレビュー

反応式

HRID 44121 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 1049PyridineHCID 78978Perfluorooctanoyl chloride

生成物 1

HCID 22280236Styrene-butadiene-styrene

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8f975e7614664bb8bfcbe4b8ea4c9b23
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541162B2

反応ノート

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