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Water → 5-Bromo-3-chloro-2-hydroxy-4-methoxybenzoic acid

HRID 629381
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HRID 629381 반응식
[Cl:1][C:2]1[C:3]([OH:13])=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:5]([OH:7])=[O:6].[Br:14]Br.O>C(O)(=O)C>[Br:14][C:9]1[C:10]([O:11][CH3:12])=[C:2]([Cl:1])[C:3]([OH:13])=[C:4]([CH:8]=1)[C:5]([OH:7])=[O:6]
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참가 물질

5

반응물 3

HCID 962WaterHCID 24408BromineHCID 847769843-Chloro-2-hydroxy-4-methoxybenzoic acid

생성물 1

HCID 1184681135-Bromo-3-chloro-2-hydroxy-4-methoxybenzoic acid수율 67.4%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a solution of 3-chloro-2-hydroxy-4-methoxybenzoic acid (11.1 g) in acetic acid (275 mL) was added bromine (8.79 g) at room temperature, and the mixture was stirred for 16 hr. To the reaction mixture was added water, and the precipitate was collected by filtration. The precipitate was washed with water, and dissolved in ethyl acetate, and the solution was washed with water and saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (10.4 g).

후처리

  1. filtrationthe precipitate was collected by filtration
  2. washThe precipitate was washed with water
  3. dissolutiondissolved in ethyl acetate
  4. washthe solution was washed with water and saturated brine
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  6. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-c0169a4f5e5149f38c2f2c304e110a3b
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315458B2

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