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2-Methoxyaniline → 4-Chloromethyl-N-(2-methoxyphenyl)benzamide

HRID 2418
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HRID 2418 반응식
[CH3:1][O:2][C:3]1[C:4]([NH2:9])=[CH:5][CH:6]=[CH:7][CH:8]=1.[OH-].[Na+].[Cl:12][CH2:13][C:14]1[CH:22]=[CH:21][C:17]([C:18](Cl)=[O:19])=[CH:16][CH:15]=1>C(Cl)Cl>[Cl:12][CH2:13][C:14]1[CH:22]=[CH:21][C:17]([C:18]([NH:9][C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=2[O:2][CH3:1])=[O:19])=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70002-MethoxyanilineHCID 14798Sodium HydroxideHCID 701364-(Chloromethyl)benzoyl chloride

생성물 1

HCID 196899684-Chloromethyl-N-(2-methoxyphenyl)benzamide수율 94.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

o-Anisidine (0.69 ml, 6.0 mmol) was dissolved in methylene chloride (10 ml) and, with cooling in an ice bath, mixed with 20% sodium hydroxide (5 ml) and 4-chloromethylbenzoyl chloride (1.17 g, 6.0 mmol). After 30 minutes of stirring at the same temperature, the reaction mixture was extracted with methylene chloride and then washed with 1N hydrochloric acid, water and saturated brine in that order. After drying on anhydrous magnesium sulfate, the solvent was removed by evaporation, and the resulting light beige solid was purified by recrystallization (ether-hexane) to obtain 1.56 g (94.2%) of the title compound in the form of colorless needle crystals.

후처리

  1. temperaturewith cooling in an ice bath
  2. extractionthe reaction mixture was extracted with methylene chloride
  3. washwashed with 1N hydrochloric acid, water and saturated brine in that order
  4. dry with materialAfter drying on anhydrous magnesium sulfate
  5. customthe solvent was removed by evaporation
  6. customthe resulting light beige solid was purified by recrystallization (ether-hexane)

출처 및 근거

ORD 기록
ord-77cb8f49e98843759fa1c7777b2640d4
출처 데이터셋
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05728835

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