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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diiodomethane → HCID 22235737, 화합물

HRID 1441045
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HRID 1441045 반응식
[CH2:1]([Zn]CC)C.[CH3:6][C:7](=[CH2:15])[CH2:8][CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11].ICI.[Cl-].[NH4+]>CCCCCC>[CH3:15][C:7]1([CH2:8][CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])[CH2:1][CH2:6]1
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6

반응물 4

HCID 6346DiiodomethaneHCID 25517Ammonium ChlorideHCID 3416433Ethyl 4-methyl-4-pentenoateHCID 178418750HCID 178418750, 화합물

생성물 1

HCID 22235737HCID 22235737, 화합물

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

Diethylzinc (40 ml. 1.1M solution in toluene) was added dropwise to a solution of ethyl 4-methylpent-4-enoate (1.25 g.) in dry hexane (100 ml.) at -20° under nitrogen After stirring for 10 minutes diiodomethane (23.6 g.) was added dropwise and the mixture maintained at -20° for 6 hours. The mixture was allowed to warm to room temperature, aqueous ammonium chloride solution (60 ml.) added and the two layers separated. The aqueous layer was extracted with diethyl ether (3×50 ml.) and the combined organic extracts washed with sodium thiosulphate solution (50 ml.) and water (50 ml.). The extracts were dried over anhydrous magnesium sulphate and evaporated in vacuo. Chromatography on silica, eluting with diethyl ether/hexane mixtures, gave ethyl 3-(1-methylcyclopropyl)propanoate as a colourless oil (1.21 g.).

후처리

  1. additionwas added dropwise
  2. temperaturethe mixture maintained at -20° for 6 hours
  3. customthe two layers separated
  4. extractionThe aqueous layer was extracted with diethyl ether (3×50 ml.)
  5. washthe combined organic extracts washed with sodium thiosulphate solution (50 ml.) and water (50 ml.)
  6. dry with materialThe extracts were dried over anhydrous magnesium sulphate
  7. customevaporated in vacuo
  8. washChromatography on silica, eluting with diethyl ether/hexane mixtures

출처 및 근거

ORD 기록
ord-23e4ee87cb1a4da8ad6e13941bc19131
출처 데이터셋
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05502073

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