Azobisisobutyronitrile → Phosphine, octyl-

HRID 261012ノート

反応式

HRID 261012 の反応式
N(C(C)(C)C#N)=NC(C)(C)C#N.[CH2:13]=[CH:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20].[PH3:21]>C1C=CC=CC=1>[CH2:13]([PH2:21])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]

参加物

5

反応物 3

HCID 6547AzobisisobutyronitrileHCID 81251-Octene2 回HCID 24404Phosphine

生成物 1

HCID 446269Phosphine, octyl-収率 70%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

反応条件

温度
90 °C

実験手順

A 1-liter autoclave was charged with 5 g of azobisisobutyronitrile, 50 g of benzene and 112 g (1 mol) of 1-octene, and 136 g (4 mols) of hydrogen phosphide was condensed thereinto. The whole was heated to 90° C. The pressure initially rose to 70 bars, then dropped gradually to 55 bars, and remained constant after 5 hours. The reaction mixture was analyzed by NMR-spectroscopy. The octene conversion rate was 85%. Primary octylphosphine was obtained in a yield of 70%, secondary octylphosphine was obtained in a yield of 20%, and tertiary octylphosphine was obtained in a yield at 10%, based on the quantity of 1-octene which underwent conversion.

後処理

  1. customcondensed
  2. additiondropped gradually to 55 bars

出典と根拠

ORDレコード
ord-d4864d5bbe6f48d9941e79dc4c7f0d38
出典データセット
uspto-grants-1979_08
特許番号
US04163760

反応ノート

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