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

Hexamethylenetetramine → 4-Methoxy-3-(trifluoromethyl)benzaldehyde

HRID 2300130
ノート
印刷プレビュー

反応式

HRID 2300130 の反応式
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH3:10].C1N2CN3CN(C2)CN1C3.FC(F)(F)[C:25](O)=[O:26]>>[F:1][C:2]([F:11])([F:12])[C:3]1[CH:8]=[C:7]([CH:6]=[CH:5][C:4]=1[O:9][CH3:10])[CH:25]=[O:26]
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 3

HCID 4101HexamethylenetetramineHCID 6422Trifluoroacetic acidHCID 27752511-Methoxy-2-(trifluoromethyl)benzene

生成物 1

HCID 27752914-Methoxy-3-(trifluoromethyl)benzaldehyde

実験手順

A mixture of 8.5 g 2-trifluoromethyl anisole and 7.0 g hexamethylene tetramine was stirred at 90° C. for 1.5 hr in 80 ml trifluoroacetic acid. The reaction solution was evaporated. The resulting residue was dissolved in ethyl acetate, and it was added dropwise into ice-cooled saturated aqueous sodium bicarbonate. The ethyl acetate layer was recovered and washed with brine. It was dried over anhydrous magnesium sulfate, filtered, and evaporated. The resulting residue was purified by silica gel column chromatography to give 5.8 g of 3-trifluoromethyl-p-anisaldehyde.

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
  • customThe reaction solution was evaporated
  • dissolutionThe resulting residue was dissolved in ethyl acetate
  • additionit was added dropwise into ice-
  • temperaturecooled saturated aqueous sodium bicarbonate
  • customThe ethyl acetate layer was recovered
  • washwashed with brine
  • dry with materialIt was dried over anhydrous magnesium sulfate
  • filtrationfiltered
  • customevaporated
  • customThe resulting residue was purified by silica gel column chromatography
  • 出典と根拠

    ORDレコード
    ord-ed346788d6fc41e588430e09a75b3d6a
    出典データセット
    uspto-grants-2002_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06498159B1

    反応ノート

    読み込み中…