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1-Hexene → Decene-1 hexene-1

HRID 4186
ノート
印刷プレビュー

反応式

HRID 4186 の反応式
C[Si](N(P(=N[Si](C)(C)C)=N[Si](C)(C)C)[Si](C)(C)C)(C)C.[CH3:21][CH2:22][CH2:23][CH2:24][CH:25]=[CH2:26]>CCCCCCCCC=C>[CH3:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:24][CH2:23][CH:22]=[CH2:21].[CH3:26][CH2:25][CH2:24][CH2:23][CH:22]=[CH2:21]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 115971-HexeneHCID 54388992Bis(trimethylsilyl)amino-bis(trimethylsilylimino)phosphorane

生成物 1

HCID 20263375Decene-1 hexene-1

試薬・触媒・溶媒 1

HCID 133811-Decene溶媒

反応条件

温度
0 °C

実験手順

In a glass vessel pre-conditioned by heating under vacuum and filled with argon 0.34 g (1.24 mmol) of bis(cyclooctadiene-1,5)nickel and 0.46 g (1.25 mmol) of bis(trimethylsilyl)amino-bis(trimethylsilylimino)phosphorane were dissolved in 20 ml of decene-1, and the solution was stirred at 0° C. for 3 hours. Then to the gel-like mass there were added 20 ml of hexene-1, and the mixture was stirred at 0° C. for another 4 hours. After a working-up procedure as described in Example 1 there were obtained 24.0 g (85% of the total amount) of a decene-1/hexene-1 block copolymer which had a methyl branching point characteristic corresponding to the molar ratio of the α-olefin reactants (Mn =1 900).

後処理

  1. temperatureIn a glass vessel pre-conditioned by heating under vacuum
  2. stirringthe mixture was stirred at 0° C. for another 4 hours

出典と根拠

ORDレコード
ord-8b39f025038f42bb9c0a692743fbf1b9
出典データセット
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04724273

反応ノート

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