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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Iodopropane → HCID 66958661, 화합물

HRID 1984379
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HRID 1984379 반응식
[CH2:1](I)[CH2:2][CH3:3].[O-]CC.[Na+].[CH2:9]([C:11]1[NH:15][N:14]=[C:13]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:12]=1)[CH3:10]>C(O)C>[CH2:2]([C:1]1[N:15]([CH2:11][CH2:9][CH3:10])[N:14]=[C:13]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH:12]=1)[CH3:3]
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참가 물질

5

반응물 3

HCID 336431-Iodopropane2회HCID 2723922Sodium ethoxide2회HCID 80276141H-Pyrazole-3-carboxylic acid, 5-ethyl-, ethyl ester

생성물 1

HCID 66958661HCID 66958661, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매3회

실험 절차

Propyl iodide (0.43 mL, 4.46 mmol) and a solution of sodium ethoxide in ethanol (21%, 0.95 g, 3.27 mmol) were added to a solution of ethyl 5-ethyl-1H-pyrazole-3-carboxylate (0.5 g, 2.97 mmol) in ethanol (5 mL) at ambient temperature. The reaction was stirred overnight, and additional propyl iodide (0.05 mL) and sodium ethoxide in ethanol (21%, 0.1 g) were added. After 3 hours, the solvent was removed under reduced pressure and the residue was partitioned between an aqueous sodium chloride solution and methyl tert-butyl ether. The aqueous phase was extracted with methyl tert-butyl ether twice. The organic phases were combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield impure ethyl 5-ethyl-1-propyl-1H-pyrazole-3-carboxylate.

후처리

  1. waitAfter 3 hours
  2. customthe solvent was removed under reduced pressure
  3. customthe residue was partitioned between an aqueous sodium chloride solution and methyl tert-butyl ether
  4. extractionThe aqueous phase was extracted with methyl tert-butyl ether twice
  5. dry with materialdried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-b88dd64dbe52455bb3d3686194366f31
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07544697B2

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