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 → HCID 22399035、化合物

HRID 1734141
ノート
印刷プレビュー

反応式

HRID 1734141 の反応式
[O:1]=[C:2]([CH3:15])[CH2:3][CH:4]([C:10](OCC)=[O:11])[C:5](OCC)=[O:6].[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1>[OH:6][CH2:5][CH:4]([CH2:3][CH:2]([OH:1])[CH3:15])[CH2:10][OH:11]
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 962WaterHCID 12000252Diethyl (2-oxopropyl)propanedioateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 22399035HCID 22399035、化合物収率 100.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 11.4 g of diethyl 2-oxopropylmalonate in 30 ml of tetrahydrofuran was added dropwise under ice-cooling over 20 minutes to a suspension of 5.00 g of lithium aluminum hydride in 100 ml of tetrahydrofuran. The reaction fluid was stirred for an hour under ice-cooling and for 4.5 hours at room temperature, and 10 ml of water was added thereto dropwise under ice-cooling over 20 minutes. The reaction fluid was refluxed for an hour and filtrated. The unfiltered solid was suspended in 200 ml of ethanol and the suspension was refluxed. The suspension was filtrated, and the filtrate combined with the foregoing filtrate was concentrated under a reduced pressure to obtain 7.08 g of 2-hydroxymethyl-1,4-pentanediol as a colorless oily matter.

後処理

  1. temperaturedropwise under ice-cooling over 20 minutes
  2. temperatureThe reaction fluid was refluxed for an hour
  3. filtrationfiltrated
  4. temperaturethe suspension was refluxed
  5. filtrationThe suspension was filtrated
  6. concentrationwas concentrated under a reduced pressure

出典と根拠

ORDレコード
ord-23dbd7f8a4a843dda0537faf08c1fcb4
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05532365

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