Hexane → 1-Cyclopentadienyl-1-(2,7-di-tert-butylfluorenyl)cyclohexane
反応式
[C:1]([C:5]1[CH:17]=[CH:16][C:15]2[C:14]3[C:9](=[CH:10][C:11]([C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:12][CH:13]=3)[CH2:8][C:7]=2[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].CCCCCC.C([Li])CCC.[CH:33]1([C:39]2[C:43](=C)[CH:42]=[CH:41][CH:40]=2)[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]1>O.C1COCC1>[CH:39]1([C:33]2([C:10]3[C:9]4[CH2:8][C:7]5[C:15](=[CH:16][CH:17]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH:6]=5)[C:14]=4[CH:13]=[CH:12][C:11]=3[C:18]([CH3:21])([CH3:20])[CH3:19])[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]2)[CH:40]=[CH:41][CH:42]=[CH:43]1参加物
実験手順
To a THF (30 ml) solution including 5.0 g (18.6 mmol) of 2,7-di-tert-butylfluorene, a hexane solution (13.5 ml, 21.6 mmol) of n-butyllithium was added dropwise at −78° C. under nitrogen, followed by stirring at room temperature for 6 hours. Next, a THF (20 ml) solution including 3.42 g (23.4 mmol) of cyclohexylfulvene was added dropwise at 0° C. under a nitrogen atmosphere, followed by stirring at room temperature for 16 hours. The resultant reaction solution was decomposed with cold water, and then extracted with ether. The extract was dried over magnesium sulfate and then filtered, and the used solvent was removed from the filtrate under reduced pressure, thereby obtaining a solid. This solid was recrystallized from methanol to obtain 5.36 g of a colorless solid.
後処理
- additionwas added dropwise at 0° C. under a nitrogen atmosphere
- stirringby stirring at room temperature for 16 hours
- customThe resultant reaction solution
- extractionextracted with ether
- dry with materialThe extract was dried over magnesium sulfate
- filtrationfiltered
- customthe used solvent was removed from the filtrate under reduced pressure
- customobtaining a solid
- customThis solid was recrystallized from methanol
出典と根拠
- ORDレコード
- ord-7c02aa446e3949f4a0b6f1a920c296a1
- 出典データセット
- uspto-grants-2002_01
- 特許番号
- US06342568B1
反応ノート
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