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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → HCID 67328702、化合物

HRID 1841832
ノート
印刷プレビュー

反応式

HRID 1841832 の反応式
[F:1]/[C:2](/[Si](CC)(CC)CC)=[C:3](/[F:13])\[CH:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][CH3:12])[CH2:6][CH2:5]1.O.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1.CC(OC)(C)C>[F:13]/[C:3](/[CH:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][CH3:12])[CH2:6][CH2:5]1)=[CH:2]/[F:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 2724141Tetrabutylammonium FluorideHCID 71074322[(Z)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]triethylsilane

生成物 1

HCID 67328702HCID 67328702、化合物

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 15413tert-Butyl methyl ether溶媒

実験手順

34.6 g (0.11 mol) of [(Z)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]triethylsilane are refluxed for 20 h in 900 ml of THF together with 45 ml of water and 160 ml of TBAF (0.16 mol, 1 M soln. in THF). The batch is diluted with MTBE and washed a number of times with water. The aqueous phases are extracted with MTBE, and the combined organic phases are washed with water and saturated sodium chloride solution. The solution is dried using sodium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography (SiO2, pentane), giving 1-((E)-1,2-difluorovinyl)-4-propylcyclohexane as a colourless oil.

後処理

  1. washwashed a number of times with water
  2. extractionThe aqueous phases are extracted with MTBE
  3. washthe combined organic phases are washed with water and saturated sodium chloride solution
  4. customThe solution is dried
  5. concentrationconcentrated under reduced pressure
  6. customThe residue is purified by column chromatography (SiO2, pentane)

出典と根拠

ORDレコード
ord-7de38795d58d4a14acea9041ea0f462f
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08945420B2

反応ノート

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