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Sodium Hydroxide → 3-Bromo-5-(3-pyridyl)benzoic Acid

HRID 2216773
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HRID 2216773 반응식
C[O:2][C:3](=[O:17])[C:4]1[CH:9]=[C:8]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:7]=[C:6]([Br:16])[CH:5]=1.[OH-].[Na+]>CO>[Br:16][C:6]1[CH:5]=[C:4]([CH:9]=[C:8]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:7]=1)[C:3]([OH:17])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 21942604Methyl-3-bromo-5-(3-pyridyl)benzoate

생성물 1

HCID 219425193-Bromo-5-(3-pyridyl)benzoic Acid수율 136.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

In a 100 ml round bottom flask equipped with stir bar added Methyl-3-bromo-5-(3-pyridyl)benzoate (1.16 g, 3.96 mmol), methanol (15 ml) and sodium hydroxide (5.94 ml, 5.94 mmol, 1N aqueous). Stirred the resulting mixture at 50° C. for 2 h. The reaction mixture was cooled to room temperature, concentrated in-vacuo and the residue was dissolved in methanol (20 ml). To this mixture added hydrochloric acid (1N diethyl ether) dropwise and stirred at room temperature for 10 min. The reaction mixture was concentrated in-vacuo and the residue was triturated with diethyl ether to provide the crude hydrochloride salt of title compound (1.50 g) as a white solid.

후처리

  1. customIn a 100 ml round bottom flask equipped
  2. stirringStirred the resulting mixture at 50° C. for 2 h
  3. concentrationconcentrated in-vacuo
  4. dissolutionthe residue was dissolved in methanol (20 ml)
  5. additionTo this mixture added hydrochloric acid (1N diethyl ether) dropwise
  6. stirringstirred at room temperature for 10 min
  7. concentrationThe reaction mixture was concentrated in-vacuo
  8. customthe residue was triturated with diethyl ether

출처 및 근거

ORD 기록
ord-02d9830f1cab48c8b612e54a446ee9bb
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07112595B2

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