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Diiodomethane → HCID 22235737、化合物

HRID 1441045
ノート
印刷プレビュー

反応式

HRID 1441045 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6346DiiodomethaneHCID 25517Ammonium ChlorideHCID 3416433Ethyl 4-methyl-4-pentenoateHCID 178418750HCID 178418750、化合物

生成物 1

HCID 22235737HCID 22235737、化合物

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

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.).

後処理

  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

出典と根拠

ORDレコード
ord-23e4ee87cb1a4da8ad6e13941bc19131
出典データセット
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05502073

反応ノート

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