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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl 3-cyclopropyl-3-(2-((methoxymethoxy)methyl)pyridin-4-yl)acrylate → Ethyl 3-cyclopropyl-3-(2-(hydroxymethyl)pyridin-4-yl)propanoate

HRID 1049476
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HRID 1049476 반응식
[CH:1]1([C:4]([C:11]2[CH:16]=[CH:15][N:14]=[C:13]([CH2:17][O:18]COC)[CH:12]=2)=[CH:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH2:3][CH2:2]1>C(O)(=O)C.[Zn]>[CH:1]1([CH:4]([C:11]2[CH:16]=[CH:15][N:14]=[C:13]([CH2:17][OH:18])[CH:12]=2)[CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH2:2][CH2:3]1
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참가 물질

4

반응물 1

HCID 131736013Ethyl 3-cyclopropyl-3-(2-((methoxymethoxy)methyl)pyridin-4-yl)acrylate

생성물 1

HCID 117759601Ethyl 3-cyclopropyl-3-(2-(hydroxymethyl)pyridin-4-yl)propanoate수율 57.2%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

To a solution of ethyl 3-cyclopropyl-3-(2-((methoxymethoxy)methyl)pyridin-4-yl)acrylate (1.28 g) in acetic acid (20 mL) was added zinc powder (2.87 g) at 20° C., and the mixture was stirred at room temperature for 10 min. The reaction mixture was filtered, and the solvent of the filtrate was evaporated under reduced pressure. The residue was dissolved in THF (30 mL), and conc. sulfuric acid (3.51 mL) was added. The reaction mixture was stirred at 60° C. for 1 hr, and further heated under reflux for 5 min. The reaction mixture was basified with aqueous potassium carbonate solution at 0° C., and extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (626 mg) as a colorless oil.

후처리

  1. filtrationThe reaction mixture was filtered
  2. customthe solvent of the filtrate was evaporated under reduced pressure
  3. dissolutionThe residue was dissolved in THF (30 mL)
  4. additionconc. sulfuric acid (3.51 mL) was added
  5. stirringThe reaction mixture was stirred at 60° C. for 1 hr
  6. temperaturefurther heated
  7. temperatureunder reflux for 5 min
  8. customwas basified with aqueous potassium carbonate solution at 0° C.
  9. extractionextracted with ethyl acetate
  10. washThe extract was washed with water and saturated brine
  11. dry with materialdried over anhydrous magnesium sulfate
  12. customThe solvent was evaporated under reduced pressure
  13. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-e5873646428740499fa6ac2b8fff41df
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09382188B2

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