反応式
[CH3:1][CH:2]=CCCCCC.[CH2:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH2:12][CH2:11][CH2:10]1.[OH:19]N1[C:24](=O)[C:23]2=[CH:26][CH:27]=[CH:28][CH:29]=[C:22]2[C:21]1=[O:30].O1C(CCCCC)C1C>[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Mo].C([O-])(=O)C.[Mn+2].C([O-])(=O)C.C(#N)C1C=CC=CC=1>[CH2:16]1[CH2:17][C:18]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:14]([OH:19])[CH2:15]1.[CH2:1]1[CH2:2][C:21](=[O:30])[C:22]2[C:23](=[CH:26][CH:27]=[CH:28][CH:29]=2)[CH2:24]1参加物
9
反応条件
- 温度
- 70 °C
実験手順
A mixture of 2 mmol of 2-octene (a mixture of cis-isomer and trans-isomer), 10 mmol of tetralin, 0.2 mmol of N-hydroxyphthalimide, 0.1 mmol of molybdenum hexacarbonyl, 0.002 mmol of manganese (II) acetate, and 2 ml of benzonitrile was stirred at 70° C. under an oxygen atmosphere (1 atm) for 5 hours. Gas chromatographic analysis of products in a reaction mixture revealed that 2-octene was converted, at a rate of 67%, into 2,3-epoxyoctane in yield of 53%. In this connection, tetralin was found to be converted, at a rate of 20%, into α-tetralol (yield: 8.2%) and α-tetralone (yield: 8.3%).
出典と根拠
- ORDレコード
- ord-bdda4ebeec7b4344ba5524132da5bb49
- 出典データセット
- uspto-grants-2001_05
- 特許番号
- US06229023B1
関連ノート
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