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2-Methoxyaniline → 3-bromo-4-chloro-N-(2-methoxy-phenyl)-benzamide

HRID 1485923
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반응식

HRID 1485923 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[Cl:11])[C:5](Cl)=[O:6].C(N(CC)CC)C.[CH3:19][O:20][C:21]1[C:22]([NH2:27])=[CH:23][CH:24]=[CH:25][CH:26]=1>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[Cl:11])[C:5]([NH:27][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=1[O:20][CH3:19])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 70002-MethoxyanilineHCID 8471TriethylamineHCID 202297303-Bromo-4-chlorobenzoyl chloride

생성물 1

HCID 686027883-bromo-4-chloro-N-(2-methoxy-phenyl)-benzamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

3-Bromo-4-chloro-benzoyl chloride in DCM (200 mL) was cooled in an ice bath and triethylamine (11.1 mol, 80 mmol) was added slowly, followed by the drop-wise addition of o-anisidine (4.5 mL, 40 mmol) in DCM (50 mL). At this time the ice bath was removed and the mixture was stirred for 12 hrs, followed by partition between DCM and water. The organic layer was washed with 1 N HCl, saturated NaHCO3, brine and dried over MgSO4. Concentration of the filtrate yielded 3-bromo-4-chloro-N-(2-methoxy-phenyl)-benzamide as a pinkish solid (13.5 g).

후처리

  1. customAt this time the ice bath was removed
  2. customby partition between DCM and water
  3. washThe organic layer was washed with 1 N HCl, saturated NaHCO3, brine
  4. dry with materialdried over MgSO4

출처 및 근거

ORD 기록
ord-951fbedf20c74039a590d4d53130edda
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422310B2

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