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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → 3-Methoxypyridine-2-carboxylic acid

HRID 1693230
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HRID 1693230 반응식
[OH-].[Na+].[CH3:3][O:4][C:5]1[C:6]([C:11]([O:13]C)=[O:12])=[N:7][CH:8]=[CH:9][CH:10]=1>CO>[CH3:3][O:4][C:5]1[C:6]([C:11]([OH:13])=[O:12])=[N:7][CH:8]=[CH:9][CH:10]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 20474189Methyl 3-methoxypyridine-2-carboxylate

생성물 1

HCID 132095403-Methoxypyridine-2-carboxylic acid수율 18.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A 5 N sodium hydroxide solution (147 μL) was added to a solution of methyl 3-methoxypyridine-2-carboxylate (112 mg) in methanol (2 mL), and the mixture was stirred at room temperature overnight. The excess of methanol was evaporated under reduced pressure, and the residue was diluted with water. The aqueous layer was washed with ether and then made weak acidic with 5 N hydrochloric acid. The aqueous layer was extracted with a THF-ethyl acetate mixed solvent, and then the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain the title compound (19 mg).

후처리

  1. customThe excess of methanol was evaporated under reduced pressure
  2. additionthe residue was diluted with water
  3. washThe aqueous layer was washed with ether
  4. extractionThe aqueous layer was extracted with a THF-ethyl acetate mixed solvent
  5. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  6. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-0790f1e12d9b43d5997abaf23c789731
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158620B2

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