反応式
[C:1]([O:13][CH3:14])(=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11].[C:15](#[N:18])[CH:16]=[CH2:17].[Na].C(C1C=CC=CC=1)(=O)C1C=CC=CC=1.CCCCCCCCCCCC.C(C=CCCCCCCCCC(OC)=O)#N>CC1C=C(C)C(N2C(=[Ru](Cl)(Cl)=CC3C=CC=CC=3OC(C)C)N(C3C(C)=CC(C)=CC=3C)CC2)=C(C)C=1.C1(C)C=CC=CC=1>[C:1]([O:13][CH3:14])(=[O:12])[CH:2]=[CH:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11].[C:15](#[N:18])[CH:16]=[CH2:17]参加物
8
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
100 mg of methyl 10-undecenoate (0.5 mmol), 53 mg of acrylonitrile (1 mmol) and 8 ml of toluene distilled over sodium-benzophenone are placed in a 50 ml second-generation Hoveyda-Grubbs catalyst dissolved in 2 ml of toluene is added, using a syringe and a syringe press, over a period of 2 hours 40 minutes, under nitrogen and with magnetic stirring. At the end of the addition, the mixture is left to react for 1 hour at 80° C. The reaction mixture is analyzed by gas chromatography (dodecane standard). The conversion of the methyl 10-undecenoate is 94%. The selectivity toward methyl 11-cyano-10-undecenoate (cis+trans mixture) is 100%. The TON is 940.
後処理
- additionis added
- additionAt the end of the addition
- waitthe mixture is left
- customto react for 1 hour at 80° C
出典と根拠
- ORDレコード
- ord-a9d9380a26bd4c04a645aa8280f1f09b
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08642792B2
関連ノート
読み込み中…