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

N,N,N',N'-Tetramethylethylenediamine → HCID 10445976、化合物

HRID 1463426
ノート
印刷プレビュー

反応式

HRID 1463426 の反応式
[CH3:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[C:4]([CH3:10])[C:3]=1[O:11][CH3:12].CN(C)CCN(C)C.C([Li])CCC.[CH:26](=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[N:29][CH:28]=1>CCOCC.CCCCCC.O>[N:29]1[CH:30]=[CH:31][CH:32]=[C:27]([CH:26]([OH:33])[C:5]2[C:4]([CH3:10])=[C:3]([O:11][CH3:12])[C:2]([CH3:1])=[CH:7][C:6]=2[O:8][CH3:9])[CH:28]=1
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

8

反応物 4

HCID 8037N,N,N',N'-TetramethylethylenediamineHCID 103713-PyridinecarboxaldehydeHCID 6433742,5-Dimethoxy-1,3-dimethylbenzeneHCID 178418339Butyllithium

生成物 1

HCID 10445976HCID 10445976、化合物

試薬・触媒・溶媒 3

HCID 962Water溶媒
HCID 3283
Diethyl Ether
溶媒
2 回
HCID 8058Hexane溶媒

反応条件

温度
-65 °C

実験手順

3.0 g of 1,3-dimethyl-2,5-dimethoxybenzene and 3.1 g of tetramethylethylenediamine were dissolved in 30 ml of dry ether and 17 ml of a 1.6M solution of n-butyllithium in hexane was added dropwise thereto in a nitrogen atmosphere at room temperature. After 1 hour, the mixture was cooled to -65° C. and a solution of 2.9 g of nicotinaldehyde in 10 ml of ether was added thereto. After 30 minutes, the reaction was ceased by adding water and the reaction mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate. After distilling off the solvent, 6.4 g of a crude product of the title compound was obtained.

後処理

  1. customat room temperature
  2. waitAfter 30 minutes
  3. extractionthe reaction mixture was extracted with ethyl acetate
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. distillationAfter distilling off the solvent, 6.4 g of a crude product of the title compound
  6. customwas obtained

出典と根拠

ORDレコード
ord-e6436a7a63314dceae549fd502051099
出典データセット
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05300518

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