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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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Bromoacetonitrile → HCID 14837015、化合物

HRID 2106805
ノート
印刷プレビュー

反応式

HRID 2106805 の反応式
[CH:1]([N:4](C(C)C)CC)(C)[CH3:2].BrCC#N.[F:14][C:15]1[C:16]([OH:28])=[N:17][CH:18]=[C:19]([O:21][C:22]([F:27])([F:26])[CH:23]([F:25])[F:24])[CH:20]=1>C(Cl)Cl>[C:1]([CH2:2][N:17]1[CH:18]=[C:19]([O:21][C:22]([F:26])([F:27])[CH:23]([F:24])[F:25])[CH:20]=[C:15]([F:14])[C:16]1=[O:28])#[N:4]
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 11534BromoacetonitrileHCID 81531DiisopropylethylamineHCID 178517845HCID 178517845、化合物

生成物 1

HCID 14837015HCID 14837015、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Diisopropylethylamine (0.82 ml, 4.7 mmol) and 0.30 ml (4.3 mmol) of bromoacetonitrile were added consecutively with stirring at ambient temperature to 3-fluoro-5-(1,1.2,2-tetrafluoroethoxy)-2-pyridinol (0.90 g, 3.98 mmol) in 5 ml of methylene chloride and the mixture allowed to react overnight. It was then diluted with 25 ml of methylene chloride, extracted with 25 ml of water and with dilute aqueous sodium carbonate, dried over sodium sulfate, and concentrated by evaporation under reduced pressure to obtain the title compound as a solid. This was recrystallized from toluene to obtain 0.92 g (86 percent of theory) of purified material melting at 75.5-77° C. The proton nmr spectrum was consistent with the assigned structure.

後処理

  1. customto react overnight
  2. extractionextracted with 25 ml of water and with dilute aqueous sodium carbonate
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated by evaporation under reduced pressure

出典と根拠

ORDレコード
ord-4c265d6afae6472590aaf47917247e5f
出典データセット
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04931452

反応ノート

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