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

2-Bromopropane → HCID 86654668、化合物

HRID 880449
ノート
印刷プレビュー

反応式

HRID 880449 の反応式
[H-].[Na+].[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[O:10])[NH:7][CH:8]=1.Br[CH:12]([CH3:14])[CH3:13]>CN(C)C=O>[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[O:10])[N:7]([CH:12]([CH3:14])[CH3:13])[CH:8]=1
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 63582-BromopropaneHCID 24758Sodium hydrideHCID 46719534-iodo-1H-pyrrole-2-carbaldehyde

生成物 1

HCID 86654668HCID 86654668、化合物収率 43.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Sodium hydride (860 mg, 55% in mineral oil, 19.7 mmol) was added to a solution of 4-iodo-pyrrole-2-carbaldehyde (3.0 g, 13.2 mmol) in dry dimethylformamide at ambient temperature under a nitrogen atmosphere. After stirring for 15 min 2-bromopropane (3.87 mL, 40.9 mmol) was added and the reaction mixture heated at reflux for 16 h. The mixture was allowed to cool to ambient temperature, quenched with water and extracted with diethyl ether. The combined organic layers were washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give a crude residue. Purification by column chromatography over silica gel (60-120 mesh) using 2% ethyl acetate in petroleum ether afforded 4-iodo-1-isopropyl-pyrrole-2-carbaldehyde (1.5 g, 43%) as a brown liquid.

後処理

  1. additionwas added
  2. temperaturethe reaction mixture heated
  3. temperatureat reflux for 16 h
  4. customquenched with water
  5. extractionextracted with diethyl ether
  6. washThe combined organic layers were washed with water, brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated in vacuo
  9. customto give a crude residue
  10. customPurification by column chromatography over silica gel (60-120 mesh)

出典と根拠

ORDレコード
ord-f4514892561e4adb88c0b1fde885f87c
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08993574B2

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