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Potassium Hydroxide → 2,7-Dichloro-9-(3,7-dimethyl-octyl)-9H-carbazole

HRID 722676
ノート
印刷プレビュー

反応式

HRID 722676 の反応式
[Cl:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Cl:15])=[CH:9][CH:10]=3)[NH:5][C:4]=2[CH:3]=1.[OH-].[K+].CCCCCCCC(C([NH3+])(C(CCCCCCC)=O)C(CCCCCCC)=O)=O.[Cl-].Br[CH2:49][CH2:50][CH:51]([CH3:58])[CH2:52][CH2:53][CH2:54][CH:55]([CH3:57])[CH3:56]>C(Cl)Cl>[Cl:1][C:2]1[CH:14]=[CH:13][C:12]2[C:11]3[C:6](=[CH:7][C:8]([Cl:15])=[CH:9][CH:10]=3)[N:5]([CH2:49][CH2:50][CH:51]([CH3:58])[CH2:52][CH2:53][CH2:54][CH:55]([CH3:57])[CH3:56])[C:4]=2[CH:3]=1
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 14797Potassium HydroxideHCID 1379141-Bromo-3,7-dimethyloctaneHCID 12070509Carbazole, 2,7-dichloro-HCID 77620884Tricaprylylmethyl ammonium chloride

生成物 1

HCID 218856252,7-Dichloro-9-(3,7-dimethyl-octyl)-9H-carbazole

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

反応条件

温度
85 °C

実験手順

2,7-Dichlorocarbazole (synthesized according to the procedure by Leclerc et al: Morin, Jean-Francois; Leclerc, Mario; Macromolecules (2001), 34(14), 4680–4682) (10.7 g, 45.3 mmol) was added to a 50% w/w aqueous solution of potassium hydroxide (75 ml) and Aliquat-336 (0.5 ml). 1-Bromo-3,7-dimethyloctane (12.0 g, 54.3 mmol) was added dropwise and the reaction mixture was heated at 85° C. for 12 h. After cooling to room temperature, methylene chloride was added. The reaction mixture was transferred to a separation funnel and the organic layer was removed. The aqueous layer was extracted with methylene chloride (3×) and the combined organic layers were dried over magnesium sulfate. After removal of the solvent in vacuo, the crude product was purified by column chromatography (silica gel, hexane) to yield 13.5 g of the product as colorless solid.

後処理

  1. temperatureAfter cooling to room temperature
  2. customThe reaction mixture was transferred to a separation funnel
  3. customthe organic layer was removed
  4. extractionThe aqueous layer was extracted with methylene chloride (3×)
  5. dry with materialthe combined organic layers were dried over magnesium sulfate
  6. customAfter removal of the solvent in vacuo
  7. customthe crude product was purified by column chromatography (silica gel, hexane)

出典と根拠

ORDレコード
ord-0712d418553b47908225e48228690562
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07138483B2

反応ノート

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