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Diethyl Ether → 1-(Methyl)-1-(3-butenyl)-1-(cyclopentadienyl)-1-(2,7-di-tert-butylfluorenyl)methane

HRID 1892070
ノート
印刷プレビュー

反応式

HRID 1892070 の反応式
[CH:1]([C:5]([CH3:11])=[C:6]1[CH:10]=[CH:9][CH:8]=[CH:7]1)=[CH:2][CH2:3][CH3:4].CCOCC.[C:17]([C:21]1[CH:33]=[CH:32][C:31]2[C:30]3[C:25](=[CH:26][C:27]([C:34]([CH3:37])([CH3:36])[CH3:35])=[CH:28][CH:29]=3)[CH2:24][C:23]=2[C:22]=1[Li])([CH3:20])([CH3:19])[CH3:18].C1C(=C)C=CC=1>CCCCC>[CH3:11][C:5]([CH2:1][CH2:2][CH:3]=[CH2:4])([CH:6]1[CH:7]=[CH:8][CH:9]=[CH:10]1)[C:33]1[C:32]2[CH2:24][C:25]3[C:30](=[CH:29][CH:28]=[C:27]([C:34]([CH3:35])([CH3:36])[CH3:37])[CH:26]=3)[C:31]=2[CH:23]=[CH:22][C:21]=1[C:17]([CH3:19])([CH3:18])[CH3:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 3283Diethyl EtherHCID 136323FulveneHCID 540533226-Butenyl-6-methylfulveneHCID 178506710HCID 178506710、化合物

生成物 1

HCID 1317264761-(Methyl)-1-(3-butenyl)-1-(cyclopentadienyl)-1-(2,7-di-tert-butylfluorenyl)methane

試薬・触媒・溶媒 1

HCID 8003Pentane
溶媒

反応条件

温度
0 °C

実験手順

Another one-liter flask fitted with an addition funnel is charged with 6-butenyl-6-methylfulvene (37 g, 253 mmol) and a stir bar, and cooled to 0° C. under a nitrogen atmosphere. The ether solution of 2,7-di-tert-butylfluorenyl lithium prepared as above is added in a dropwise fashion to the fulvene at 0° C. via the addition funnel over the course of approximately one hour. The resulting dark-colored reaction mixture is warmed to room temperature and stirred overnight (at least about 12 hours) under a nitrogen atmosphere. The reaction mixture is then quenched with the slow addition of a saturated NH4Cl/H2O solution (300 mL), the organic layer extracted with ether, washed twice with H2O (500 mL), dried over anhydrous Na2SO4, filtered, and the filtrate evaporated to dryness. The crude product obtained by this method is then dissolved in pentane and maintained at about 0° C. in a freezer, thereby affording the product as a white solid that is washed with cold pentane, dried under vacuum, and isolated and used without further purification. Further product could be isolated in smaller quantities through concentrating the mother liquors and combined washings and placing them back in freezer.

後処理

  1. customAnother one-liter flask fitted with an addition funnel
  2. temperatureThe resulting dark-colored reaction mixture is warmed to room temperature
  3. customThe reaction mixture is then quenched with the slow addition of a saturated NH4Cl/H2O solution (300 mL)
  4. extractionthe organic layer extracted with ether
  5. washwashed twice with H2O (500 mL)
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. customthe filtrate evaporated to dryness
  9. customThe crude product obtained by this method
  10. temperaturemaintained at about 0° C. in a freezer

出典と根拠

ORDレコード
ord-8d31b7dfc50647d9a2e32cf4f03fceb2
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08507621B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート