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

Water → 2-Isobutylpent-4-en-1-ol

HRID 551638
ノート
印刷プレビュー

反応式

HRID 551638 の反応式
[CH2:1]([CH:5]([CH2:9][CH:10]=[CH2:11])[C:6](O)=[O:7])[CH:2]([CH3:4])[CH3:3].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[CH2:1]([CH:5]([CH2:9][CH:10]=[CH2:11])[CH2:6][OH:7])[CH:2]([CH3:4])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962Water2 回HCID 14798Sodium HydroxideHCID 130107432-(2-Methylpropyl)pent-4-enoic acidHCID 21226445Aluminium lithium hydride

生成物 1

HCID 866461312-Isobutylpent-4-en-1-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

2-isobutyl-4-pentenoic acid (J. Am. Chem. Soc. 115, 1993, 8669) (13 g, 83 mmol) was dissolved in tetrahydrofuran (80 mL), and the solution was added dropwise to a tetrahydrofuran (80 mL) mixed solution of lithium aluminum hydride (3.4 g, 90 mmol) under ice cooling. The mixture was stirred at this temperature for 1 hour. Then, water (3.4 mL), a 15% aqueous sodium hydroxide solution (3.4 mL), and water (10.2 mL) were added thereto in this order, and the mixture was stirred overnight. After removal of insoluble matter, the filtrate was concentrated to obtain the compound of interest as an oil substance (4.9 g, 42%).

後処理

  1. stirringin this order, and the mixture was stirred overnight
  2. customAfter removal of insoluble matter
  3. concentrationthe filtrate was concentrated
  4. customto obtain the compound of interest as an oil substance (4.9 g, 42%)

出典と根拠

ORDレコード
ord-91bb5a849bba4df89c330b3a5f1fd770
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07947738B2

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