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

Formic Acid → HCID 14211280、化合物

HRID 377125
ノート
印刷プレビュー

反応式

HRID 377125 の反応式
[CH3:1][C:2]1[N:7]=[C:6]([CH2:8][CH2:9][O:10][C:11]2[CH:12]=[CH:13][CH:14]=[C:15]([CH:18]=2)C#N)[CH:5]=[CH:4][CH:3]=1.[CH:19](O)=[O:20]>[Ni]>[CH3:1][C:2]1[N:7]=[C:6]([CH2:8][CH2:9][O:10][C:11]2[CH:18]=[CH:15][C:14]([CH:19]=[O:20])=[CH:13][CH:12]=2)[CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 284Formic AcidHCID 193574065-[2-(6-Methyl-2-pyridyl)ethoxy]benzonitrile

生成物 1

HCID 14211280HCID 14211280、化合物

試薬・触媒・溶媒 1

HCID 935Nickel触媒

実験手順

A mixture of 5-[2-(6-methyl-2-pyridyl)ethoxy]benzonitrile (9.62 g), Raney nickel alloy (10.0 g) and 75% formic acid (150 ml) was heated under reflux for 1 hour. The reaction mixture was filtered and the filtrate was concentrated. The residue was diluted with water, alkalinized with 4N-KOH, and extracted with ethyl ether. The ethyl ether layer was washed with water and dried (MgSO4) and the solvent was distilled off. The residue was recrystallized from ethyl etherhexane to give 4-[2-(6-methyl-2-pyridyl)ethoxy]benzaldehyde.

後処理

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
  1. temperaturewas heated
  2. temperatureunder reflux for 1 hour
  3. filtrationThe reaction mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. additionThe residue was diluted with water
  6. extractionextracted with ethyl ether
  7. washThe ethyl ether layer was washed with water
  8. dry with materialdried (MgSO4)
  9. distillationthe solvent was distilled off
  10. customThe residue was recrystallized from ethyl etherhexane

出典と根拠

ORDレコード
ord-d316f452bab342edb824538507be3703
出典データセット
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE036575

反応ノート

読み込み中…