反応式
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1.C=CC1C=CC=CC=1.C1C=CC=CC=1.N(C(C)(C)C#N)=NC(C)(C)C#N>C(O)C>[CH2:7]=[CH:6][C:5]1[CH:8]=[CH:9][CH:2]=[CH:3][CH:4]=1.[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1参加物
6
実験手順
A solution of 13.9 g. 4-chlorostyrene and 10.4 g. styrene in 120 ml. dry benzene containing 0.24 g. azobisisobutyronitrile (Vazo® 64, du Pont) was stirred under nitrogen at 58°-64° C. for 24 hours. The solution was solvent stripped to a colorless syrupy residue which was dissolved in 50 ml. benzene and the solution added slowly with stirring to 300 ml. absolute ethanol. The precipitated polymer was filtered, washed with ethanol, and dried. The yield was 15.2 g. Analysis of the polymer showed presence of 15.83% chlorine, equivalent to a copolymer containing 47 mole % styrene and 53 mole % 4-chlorostyrene units in the repeat unit.
後処理
- dissolutionwas dissolved in 50 ml
- filtrationThe precipitated polymer was filtered
- washwashed with ethanol
- customdried
- additioncontaining 47 mole % styrene and 53 mole % 4-chlorostyrene units in the repeat unit
出典と根拠
- ORDレコード
- ord-6598418db32d4962aeed2923ab4eb26b
- 出典データセット
- uspto-grants-1983_03
- 特許番号
- US04375461
関連ノート
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