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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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Azobisisobutyronitrile → HCID 11249951、化合物

HRID 901818
ノート
印刷プレビュー

反応式

HRID 901818 の反応式
[F:1][C:2](I)([F:31])[C:3]([F:30])([F:29])[C:4]([F:28])([F:27])[C:5]([F:26])([F:25])[C:6]([F:24])([F:23])[C:7]([F:22])([F:21])[C:8]([F:20])([F:19])[C:9]([F:18])([F:17])[C:10]([F:16])([F:15])[C:11]([F:14])([F:13])[F:12].[CH2:33]([Sn](CCCC)(CCCC)CCCC)[CH:34]=[CH2:35].CC(N=NC(C#N)(C)C)(C#N)C>CCCCCC>[F:1][C:2]([F:31])([CH2:35][CH:34]=[CH2:33])[C:3]([F:30])([F:29])[C:4]([F:28])([F:27])[C:5]([F:26])([F:25])[C:6]([F:24])([F:23])[C:7]([F:22])([F:21])[C:8]([F:20])([F:19])[C:9]([F:18])([F:17])[C:10]([F:16])([F:15])[C:11]([F:14])([F:13])[F:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6547AzobisisobutyronitrileHCID 67920Perfluorodecyl iodideHCID 90628Allyltributylstannane

生成物 1

HCID 11249951HCID 11249951、化合物収率 97%

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

In a typical procedure for reverse fluorous solid phase extraction in the studies of FIG. 4, a perfluoroalkyl iodide such as perfluorodecyl iodide (RfI, 323 mg, 0.5 mmol), allyltributyltin (330 mg, 1 mmol), AIBN (9 mg, 0.05 mmol) and hexane (5 ml) were placed in a flask under an argon atmosphere and the mixture was refluxed for 5 h. After removal of the volatile components by evaporation, the mixture was submitted to separation by reverse fluorous solid phase extraction. A short column was packed with regular silica gel (6.0 g) using FC-72/Et2O (2/1) as the solvent. The crude reaction mixture was then loaded onto this column and eluted with 20 ml of FC-72/Et2O (2/1) to give 3-(perfluorodecyl)prop-1-ene in 97% yield (271 mg). After similar reactions and separations, the allylated products 2a-d, 3a-d and 4a-d were isolated in yields ranging from 69-93%. The nuclear magnetic resonance (NMR) spectra of these products were clean, and gas chromatography (GC) or high pressure liquid chromatography (HPLC) purities exceeded 90% in all cases. The purity of the products was determined by GC in the case of R═H or R═Me and HPLC (Nova Pak® Silica, UV detection at 254 nm) in the case of R═Ph.

後処理

  1. extractionIn a typical procedure for reverse fluorous solid phase extraction in the studies of FIG. 4
  2. temperaturethe mixture was refluxed for 5 h
  3. customAfter removal of the volatile components
  4. customby evaporation
  5. customthe mixture was submitted to separation by reverse fluorous solid phase extraction
  6. customThe crude reaction mixture
  7. washeluted with 20 ml of FC-72/Et2O (2/1)

出典と根拠

ORDレコード
ord-62ecb49063c34ababe95f7a6e41f56b0
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07364908B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート