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Sodium Hydroxide → (E)-4-(2-(1H-indazol-3-yl)vinyl)benzoic acid

HRID 2075431
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반응식

HRID 2075431 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3](/[CH:10]=[CH:11]/[C:12]2[CH:21]=[CH:20][C:15]([C:16]([O:18]C)=[O:17])=[CH:14][CH:13]=2)=[N:2]1.[OH-].[Na+]>CO>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3](/[CH:10]=[CH:11]/[C:12]2[CH:21]=[CH:20][C:15]([C:16]([OH:18])=[O:17])=[CH:14][CH:13]=2)=[N:2]1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 11952156methyl (E)-4-[2-(1H-indazol-3-yl)vinyl]benzoate

생성물 1

HCID 11437002(E)-4-(2-(1H-indazol-3-yl)vinyl)benzoic acid수율 104.3%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Methyl (E)-4-[2-(H-indazol-3-yl)vinyl]benzoate (0.71 g, 2.54 mmol) obtained in Step 5 was dissolved in methanol (2.6 mL), and the solution was added with an aqueous sodium hydroxide solution (1 mol/L, 5.00 mL), followed by heating under reflux for 1.5 hours. Methanol was evaporated under reduced pressure, the pH of the residue was adjusted to 3 or below with 6 mol/L hydrochloric acid under ice-cooling. The resulting precipitates were collected by filtration to obtain (E)-4-[2-(1H-indazol-3-yl)vinyl]benzoic acid (0.70 g, quantitative yield).

후처리

  1. temperatureby heating
  2. temperatureunder reflux for 1.5 hours
  3. customMethanol was evaporated under reduced pressure
  4. temperaturecooling
  5. customThe resulting precipitates
  6. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-994a18ea12d540b1ba101b0d333a3f72
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07919517B2

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