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Benzoyl chloride → N-[2-(4-bromophenylamino)phenyl]benzamide

HRID 2405453
ノート
印刷プレビュー

反応式

HRID 2405453 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[N+:15]([O-])=O)=[CH:4][CH:3]=1.S(S([O-])=O)([O-])=O.[Na+].[Na+].C(=O)([O-])O.[Na+].[C:31](Cl)(=[O:38])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>O1CCCC1.O.C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[NH:15][C:31](=[O:38])[C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)=[CH:4][CH:3]=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 4

HCID 7412Benzoyl chlorideHCID 24489Sodium DithioniteHCID 516892Sodium BicarbonateHCID 12000290N-(4-bromophenyl)-2-nitroaniline

生成物 1

HCID 23160217N-[2-(4-bromophenylamino)phenyl]benzamide収率 45%

試薬・触媒・溶媒 3

HCID 962Water
溶媒
2 回
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒2 回

実験手順

3.8 g (13 mmol) of (4-bromophenyl)-(2-nitrophenyl)amine was dissolved in 30 mL of tetrahydrofuran. A solution of 11 g (64 mmol) of sodium hydrosulfite in 30 mL of water was added dropwise to the solution while stirring the solution at room temperature in an argon atmosphere. After stirring the mixture for 5 hours, 20 mL of ethyl acetate was added to the mixture. A solution of 2.2 g (26 mmol) of sodium hydrogencarbonate in 20 mL of water was then added to the mixture. After the dropwise addition of a solution of 2.5 g (18 mmol) of benzoyl chloride in 10 mL of ethyl acetate, the mixture was stirred at room temperature for 1 hour. The mixture was then extracted with ethyl acetate, washed with water and a saturated sodium chloride solution sequentially, and dried over anhydrous sodium sulfate. The solvent was then evaporated under reduced pressure to obtain 2.1 g of N-[2-(4-bromophenylamino)phenyl]benzamide (yield: 45%).

後処理

  1. stirringAfter stirring the mixture for 5 hours
  2. stirringthe mixture was stirred at room temperature for 1 hour
  3. extractionThe mixture was then extracted with ethyl acetate
  4. washwashed with water
  5. dry with materiala saturated sodium chloride solution sequentially, and dried over anhydrous sodium sulfate
  6. customThe solvent was then evaporated under reduced pressure

出典と根拠

ORDレコード
ord-9fe67d37f5394597be7cd2fbcafceadf
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08803420B2

反応ノート

読み込み中…

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