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

4-Bromoaniline → N-(4-bromophenyl)-3-(3-chlorophenyl)propanamide

HRID 928737
ノート
印刷プレビュー

反応式

HRID 928737 の反応式
C(N(CC)CC)C.[Br:8][C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=1.[Cl:16][C:17]1[CH:18]=[C:19]([CH2:23][CH2:24][C:25](O)=[O:26])[CH:20]=[CH:21][CH:22]=1.CCN=C=NCCCN(C)C.C([O-])(O)=O.[Na+]>C(Cl)Cl.O>[Br:8][C:9]1[CH:15]=[CH:14][C:12]([NH:13][C:25](=[O:26])[CH2:24][CH2:23][C:19]2[CH:20]=[CH:21][CH:22]=[C:17]([Cl:16])[CH:18]=2)=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 78074-BromoanilineHCID 8471TriethylamineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 1771643-(3-Chlorophenyl)propanoic acidHCID 516892Sodium Bicarbonate

生成物 1

HCID 1407353N-(4-bromophenyl)-3-(3-chlorophenyl)propanamide

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344Dichloromethane溶媒2 回

実験手順

Triethylamine (1.01 mL, 7.27 mmol) was added slowly to a mixture of 4-bromoaniline (0.500 g, 2.91 mmol), 3-(3-chlorophenyl)propanoic acid (0.643 g, 2.91 mmol), and EDCI (0.669 g, 3.49 mmol) in CH2Cl2 (20 mL). The mixture was stirred at room temperature for 48 hours and saturated aqueous NaHCO3 was added. Water (50 mL) was added followed by additional CH2Cl2. The mixture as stirred for 10 minutes and layers were separated. The CH2Cl2 layer was dried over Na2SO4, then filtered. The solvent was removed under reduced pressure and the residual oil chromatographed (CH2Cl2/EtOAc) to provide the title compound as a white fluffy solid.

後処理

  1. stirringThe mixture as stirred for 10 minutes
  2. customlayers were separated
  3. dry with materialThe CH2Cl2 layer was dried over Na2SO4
  4. filtrationfiltered
  5. customThe solvent was removed under reduced pressure
  6. customthe residual oil chromatographed (CH2Cl2/EtOAc)

出典と根拠

ORDレコード
ord-b4fdfe9ea8fa4d4f871665aa31bd806d
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09290476B2

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