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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium hydride → 1-[1-(4-Methylphenyl)cyclopropyl]ethan-1-one

HRID 1166616
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인쇄 미리보기

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HRID 1166616 반응식
[H-].[Na+].[I-].[CH3:4][S+](C)C.[CH3:8][C:9]1[CH:14]=[CH:13][C:12]([C:15](=[CH2:19])[C:16](=[O:18])[CH3:17])=[CH:11][CH:10]=1>CN(C)C=O>[CH3:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2([C:16](=[O:18])[CH3:17])[CH2:4][CH2:19]2)=[CH:11][CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24758Sodium hydrideHCID 75127Trimethylsulfonium iodideHCID 180007733-(4-Methylphenyl)-3-buten-2-one

생성물 1

HCID 180009341-[1-(4-Methylphenyl)cyclopropyl]ethan-1-one수율 48.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

반응 조건

온도
0 °C

실험 절차

507 mg of sodium hydride (55% in paraffin oil) is introduced into 20 ml of dimethylformamide under nitrogen at 0° C., and 1.36 g of trimethylsulfonium iodide is added. After 30 minutes at this temperature, 845 mg of ketone 40 is added in drops to 4 ml of dimethylformamide. It is stirred for 1 more hour at 0° C., then quenched with sodium chloride solution, extracted with ethyl acetate, dried on sodium sulfate and concentrated by evaporation. After chromatography on silica gel with ethyl acetate/hexane, 447 mg of title compound 41 is obtained as a colorless oil.

후처리

  1. customquenched with sodium chloride solution
  2. extractionextracted with ethyl acetate
  3. customdried on sodium sulfate
  4. concentrationconcentrated by evaporation

출처 및 근거

ORD 기록
ord-089d14185eaa43a49db8aa7f0321f97c
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06613920B1

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