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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Iodoethane → 5-Ethoxy-2-methylpyridine

HRID 980549
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HRID 980549 반응식
[H-].[Na+].[OH:3][C:4]1[CH:5]=[CH:6][C:7]([CH3:10])=[N:8][CH:9]=1.[CH2:11](I)[CH3:12]>CN(C)C=O.O>[CH2:11]([O:3][C:4]1[CH:5]=[CH:6][C:7]([CH3:10])=[N:8][CH:9]=1)[CH3:12]
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참가 물질

6

반응물 3

HCID 6340IodoethaneHCID 142752-Methyl-5-hydroxypyridineHCID 24758Sodium hydride

생성물 1

HCID 5731985-Ethoxy-2-methylpyridine

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매2회

실험 절차

To a stirred suspension of 16.6 g sodium hydride in 500 ml dry dimethylformamide (DMF) under nitrogen at 0° C. is added 90 g 5-hydroxy-2-methylpyridine at such a rate that the temperature remains between 0°-5° C. When gas evolution ceases, 73.8 ml ethyl iodide in 100 ml DMF is added dropwise. After stirring at room temperature overnight, the mixture is diluted with water and extracted with ether. The ether extracts are washed with brine, dried and concentrated. This oil is distilled to give 62.5 g of 5-ethoxy-2-methylpyridine, bp 89°-91° C. at 12 mm.

후처리

  1. customremains between 0°-5° C
  2. extractionextracted with ether
  3. washThe ether extracts are washed with brine
  4. customdried
  5. concentrationconcentrated
  6. distillationThis oil is distilled

출처 및 근거

ORD 기록
ord-c926faa744fc4cb8bc733a3677ac6075
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04638068

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