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

3-Fluorobenzaldehyde → 2-[(3-fluorophenyl)(hydroxy)methyl]-4-methoxy-N-methylbenzamide

HRID 2196385
ノート
印刷プレビュー

反応式

HRID 2196385 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:6]([C:7]([NH:9][CH3:10])=[O:8])=[CH:5][CH:4]=1.[Li]CCCC.[F:18][C:19]1[CH:20]=[C:21]([CH:24]=[CH:25][CH:26]=1)[CH:22]=[O:23]>C1COCC1>[F:18][C:19]1[CH:20]=[C:21]([CH:22]([OH:23])[C:11]2[CH:12]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=2[C:7]([NH:9][CH3:10])=[O:8])[CH:24]=[CH:25][CH:26]=1
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 680093-FluorobenzaldehydeHCID 3460314-methoxy-N-methylbenzamideHCID 178418339Butyllithium

生成物 1

HCID 685140052-[(3-fluorophenyl)(hydroxy)methyl]-4-methoxy-N-methylbenzamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a −78 C solution of 4-methoxy-N-methylbenzamide (2.0 g) in THF was added n-BuLi (10 mL, 2.5 M in hexanes). The reaction was stirred for 10 min at −78 C, warmed to 0 C, then cooled back to −78 C. 3-fluorobenzaldehyde (1.90 mL) was added as a solution in THF via cannula. The reaction was warmed to room temp, then quenched with saturated aqueous NH4Cl. The mixture was extracted with EtOAc, concentrated, and purified by flash chromatography (5% MeOH in CH2Cl2) to give 2-[(3-fluorophenyl) (hydroxy)methyl]-4-methoxy-N-methylbenzamide.

後処理

  1. temperaturewarmed to 0 C
  2. temperaturecooled back to −78 C
  3. customquenched with saturated aqueous NH4Cl
  4. extractionThe mixture was extracted with EtOAc
  5. concentrationconcentrated
  6. custompurified by flash chromatography (5% MeOH in CH2Cl2)

出典と根拠

ORDレコード
ord-55dcba5398b54fcaafb57ab57cf1f501
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08338449B2

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