2-Allylphenol → o-Allylphenol 1,3-bisglycidylresorcinol

HRID 414146ノート

反応式

HRID 414146 の反応式
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH:2]=[CH2:3].[CH2:11]([C:15]1([CH:22]=[CH:21][CH2:20][C:18]([CH2:23][CH:24]2[O:26][CH2:25]2)([OH:19])[CH2:17]1)[OH:16])[CH:12]1[O:14][CH2:13]1.[I-].C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)C[PH3+])C=CC=CC=1.CC(O)C([O-])=O>>[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH:2]=[CH2:3].[CH2:23]([C:18]1([CH:20]=[CH:21][CH2:22][C:15]([CH2:11][CH:12]2[O:14][CH2:13]2)([OH:16])[CH2:17]1)[OH:19])[CH:24]1[O:26][CH2:25]1

参加物

5

反応条件

温度
140 °C

実験手順

In a similar manner to that described in Example 1, o-allylphenol (134 g), 1,3-bisglycidylresorcinol (115.1 g), triphenylethylphosphonium iodide (0.75 g) and methylglycolate (145 g) were reacted at 100° C. for 13 hours. The solvent and excess o-allylphenol were removed by heating at 140° C. finally in vacuo. The yield of adduct was 227.9 g and it showed a viscosity of 280 mPa.s at 70° C.

後処理

  1. customwere reacted at 100° C. for 13 hours
  2. customThe solvent and excess o-allylphenol were removed
  3. customat 70° C.

出典と根拠

ORDレコード
ord-e6801e61cf86454d8311729680bdb68f
出典データセット
uspto-grants-1988_12
特許番号
US04789704

反応ノート

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