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

2-Ethoxybenzoyl chloride → 2-(Ethoxybenzamido)-3-methoxybenzamide

HRID 412033
ノート
印刷プレビュー

反応式

HRID 412033 の反応式
[CH2:1]([O:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6](Cl)=[O:7])[CH3:2].[NH2:13][C:14]1[C:22]([O:23][CH3:24])=[CH:21][CH:20]=[CH:19][C:15]=1[C:16]([NH2:18])=[O:17]>N1C=CC=CC=1>[CH2:1]([O:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6]([NH:13][C:14]1[C:22]([O:23][CH3:24])=[CH:21][CH:20]=[CH:19][C:15]=1[C:16]([NH2:18])=[O:17])=[O:7])[CH3:2]
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 2

HCID 30163972-Ethoxybenzoyl chlorideHCID 185365712-Amino-3-methoxybenzamide

生成物 1

HCID 185365662-(Ethoxybenzamido)-3-methoxybenzamide収率 54.3%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

2-Ethoxybenzoyl chloride (8.9 g, 0.048 mol) was added dropwise to a stirred solution of 2-amino-3-methoxybenzamide (4.0 g, 0.024 mol) in pyridine (35 ml) under a nitrogen atmosphere at 0° C. After 20 hours at room temperature, the solvent was removed by evaporation under vacuum, the residue dissolved in dichloromethane (100 ml) and the solution washed successively with 2N hydrochloric acid (2×100 ml) and saturated aqueous sodium hydrogen carbonate solution (2×100 ml). The organic phase was dried (MgSO4) and evaporated under vacuum, then the resulting oil chromatographed on silica gel (40 g), eluting with a mixture of methanol in-dichloromethane (2%), to give the title compound as a colourless solid (4.1 g, 54%), m.p. 177-179° C.

後処理

  1. customthe solvent was removed by evaporation under vacuum
  2. dissolutionthe residue dissolved in dichloromethane (100 ml)
  3. washthe solution washed successively with 2N hydrochloric acid (2×100 ml) and saturated aqueous sodium hydrogen carbonate solution (2×100 ml)
  4. dry with materialThe organic phase was dried (MgSO4)
  5. customevaporated under vacuum
  6. customthe resulting oil chromatographed on silica gel (40 g)
  7. washeluting with a mixture of methanol in-dichloromethane (2%)

出典と根拠

ORDレコード
ord-588c7520f5b14ee59b32827024981d1c
出典データセット
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06562830B1

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