ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Isobutyronitrile → 2-(6-Bromopyridin-2-yl)-2-methylpropanenitrile

HRID 384047
ノート
印刷プレビュー

反応式

HRID 384047 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:11](#[N:15])[CH:12]([CH3:14])[CH3:13].Br[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([Br:23])[N:18]=1>C1(C)C=CC=CC=1.CCOCC>[Br:23][C:19]1[N:18]=[C:17]([C:12]([CH3:14])([CH3:13])[C:11]#[N:15])[CH:22]=[CH:21][CH:20]=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 3

HCID 6559IsobutyronitrileHCID 122742,6-DibromopyridineHCID 3251421Potassium bis(trimethylsilyl)amide

生成物 1

HCID 579696582-(6-Bromopyridin-2-yl)-2-methylpropanenitrile収率 65.5%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒2 回HCID 3283Diethyl Ether
溶媒

反応条件

温度
0 °C

実験手順

Potassium bis(trimethylsilyl)amide (0.5 M in toluene, 200 ml, 100 mmol) was added slowly to a solution of isobutyronitrile (8.55 ml, 95.26 mmol) in toluene (200 ml) cooled down to 0° C. After complete addition, the reaction mixture was allowed to warm up to room temperature over 1 hour. The resulting mixture was added to a solution of 2,6-dibromopyridine (56.42 g, 238.15 mmol) in toluene (100 ml). The reaction mixture was stirred at room temperature for 18 hours. The crude mixture was diluted with ether, washed with a saturated aqueous solution of ammonium chloride and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as an oil (14.04 g, 65% yield).

後処理

  1. additionAfter complete addition
  2. temperatureto warm up to room temperature over 1 hour
  3. washwashed with a saturated aqueous solution of ammonium chloride and brine
  4. dry with materialThe organic phase was dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified on silica gel by flash column chromatography

出典と根拠

ORDレコード
ord-ccc80749565e4d3a8e5cc79fee5e0763
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367697B2

反応ノート

読み込み中…

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