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

Sodium Iodide → 5-Ethyl-2-pyridinol

HRID 1438316
ノート
印刷プレビュー

反応式

HRID 1438316 の反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH2:10])=[CH:5][N:4]=1.[Na+].[I-]>CO.[Pd]>[CH2:9]([C:6]1[CH:7]=[CH:8][C:3](=[O:2])[NH:4][CH:5]=1)[CH3:10]
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

5

反応物 2

HCID 5238Sodium IodideHCID 230701355-Ethenyl-2-methoxypyridine

生成物 1

HCID 193658715-Ethyl-2-pyridinol収率 83%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

反応条件

温度
65 °C

実験手順

To a solution of 2-methoxy-5-vinyl-pyridine (2 g) in anhydrous MeOH was added Pd/C (10 wt %, 100 mg). The mixture was stirred under H2 atmosphere for 5 hours before it was filtered through a pad of celite. The solvent was removed in vacuo and the residue was taken directly into next step without further purification. The crude product from previous step was dissolved in anhydrous MeCN. To this solution was added NaI (3.3 g, 21.9 mmol) and TMSCI (2.8 mL, 21.9 mmol). The resulting mixture was heated to 65° C. for 5 hours before it was filtered through a pad of celite. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography to afford the desired product (1.5 g, 83% yield). 1H NMR (300 MHz, CDCl3): δ 1.17 (t, J=7.5 Hz, 3H), 2.39-2.49 (m, 2H), 6.50-6.58 (m, 1H), 7.15 (s, 1H), 7.35-7.45 (m, 1H).

後処理

  1. filtrationwas filtered through a pad of celite
  2. customThe solvent was removed in vacuo
  3. customthe residue was taken directly into next step without further purification
  4. dissolutionThe crude product from previous step was dissolved in anhydrous MeCN
  5. filtrationwas filtered through a pad of celite
  6. concentrationThe filtrate was concentrated in vacuo
  7. customthe residue was purified by flash column chromatography

出典と根拠

ORDレコード
ord-b1822e24b3a34028a2fc06ad2ea123b2
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07622605B2

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