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4-Chlorophenyl acrylate → HCID 9989898、化合物

HRID 1871181
ノート
印刷プレビュー

反応式

HRID 1871181 の反応式
C(OC1C=CC([Cl:12])=CC=1)(=O)C=C.[C:13]([O-:26])(=O)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]CCCCCC.[C:27]([O-:40])(=O)[CH2:28][CH2:29]CCCCCCCCC.C([Sn+2]CCCC)CCC>>[C:27]([O:26][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:18]=1[Cl:12])(=[O:40])[CH:28]=[CH2:29]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 2934614-Chlorophenyl acrylateHCID 9809426Di-n-butyldilauryltin

生成物 1

HCID 9989898HCID 9989898、化合物

実験手順

A solution was prepared containing 98.86 wt. % 4-chlorophenyl acrylate and 1.14 wt. % dibutyltin dilaurate. 0.017 g of this solution was added to a vial containing 0.2519 g diisocyanate-terminated polypropylene glycol (MW=2471), 0.047 g α,ω-dihydroxypolypropylene glycol (MW=425), 0.051 g 4-chlorophenyl acrylate, and 0.00063 g Ciba CGI-784 (photoinitiator). The mixture was thoroughly mixed and allowed to cure overnight at room temperature, while protected from light. The polymerization was a step polymerization of the isocyanate groups with the hydroxyl groups to form a polyurethane with dissolved chlorophenyl acrylate monomer. The mixture appeared clear and transparent to the naked eye. Upon exposure to an intense tungsten light, which initiated polymerization of the acrylate monomer, the sample remained clear and transparent, indicating the compatibility of the monomer and the matrix polymer.

後処理

  1. custom
A solution was prepared
  • customterminated polypropylene glycol (MW=2471), 0.047 g α,ω-dihydroxypolypropylene glycol (MW=425), 0.051 g 4-chlorophenyl acrylate, and 0.00063 g Ciba CGI-784 (photoinitiator)
  • additionThe mixture was thoroughly mixed
  • customa step polymerization of the isocyanate groups with the hydroxyl groups
  • 出典と根拠

    ORDレコード
    ord-45d65e38b27e4db48457e30e5e1eb163
    出典データセット
    uspto-grants-2000_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06103454

    反応ノート

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