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

HRID 2405453
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HRID 2405453 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

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

생성물 1

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

시약·촉매·용매 3

HCID 962Water
용매
2회
HCID 8028Tetrahydrofuran용매
HCID 8857Ethyl Acetate용매2회

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-9fe67d37f5394597be7cd2fbcafceadf
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08803420B2

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