Styrene → 1-Heptene

HRID 495681

反応式

HRID 495681 の反応式
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C1COCC1>[CH2:1]=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH:2]([CH:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)=[CH2:1]

参加物

4

反応物 1

HCID 7501Styrene

生成物 2

HCID 116101-HepteneHCID 12757Vinylcyclohexane

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

The catalysts of the invention are effective and practical chiral catalysts for enantioselective metathesis. Examples of AROM/CM reactions catalyzed by chiral catalysts of the invention are shown in Table 1. As shown in Example 1, treatment of 19 with 5 equivalents of styrene in the presence of 10 mol % catalyst 9 in THF (50° C.) leads to the formation of 20a in 80% ee and 71% isolated yield (>98% trans). Ru-catalyzed AROM/CM is highly selective with aliphatic olefins. With aliphatic olefins such as 1-heptene and sterically bulky vinylcyclohexane (entries 2-3), 20b-c are obtained in >98% ee, >98% trans and 57-60% yield.

後処理

  1. customisolated
  2. customyield (>98% trans)

出典と根拠

ORDレコード
ord-7f06d68ce0af49cea785a59f32070a09
出典データセット
uspto-grants-2005_09
特許番号
US06939982B2

関連ノート

読み込み中…