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Hydrochloric Acid → 5-Cyclohexyl-2,2-dimethyl-5-(1-hydroxyethyl)-1,3-dioxane

HRID 2372416
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HRID 2372416 반응식
[CH3:1][Mg]I.[CH:4]1([C:10]2([CH:18]=[O:19])[CH2:15][O:14][C:13]([CH3:17])([CH3:16])[O:12][CH2:11]2)[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1.Cl>CCOCC>[CH:4]1([C:10]2([CH:18]([OH:19])[CH3:1])[CH2:15][O:14][C:13]([CH3:16])([CH3:17])[O:12][CH2:11]2)[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9]1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 199044255-Cyclohexyl-2,2-dimethyl-5-formyl-1,3-dioxaneHCID 178418373HCID 178418373, 화합물

생성물 1

HCID 199043995-Cyclohexyl-2,2-dimethyl-5-(1-hydroxyethyl)-1,3-dioxane

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Methyl magnesium iodide (3.0 ml, 3M solution in ether) was added to a solution of 5-cyclohexyl-2,2-dimethyl-5- formyl-1,3-dioxane (1.8 g.) in dry ether (50 ml.) The mixture was refluxed, with stirring, for two hours, cooled and poured into a mixture of 2N hydrochloric acid solution in ice. The aqueous mixture was extracted with ether. The ether extracts were washed with water, dried over anhydrous magnesium sulphate and evaporated in vacuo. 5-Cyclohexyl-2,2-dimethyl-5-(1-hydroxyethyl)-1,3-dioxane was obtained as a cream solid (1.5 g.)

후처리

  1. temperaturewas refluxed
  2. temperaturecooled
  3. extractionThe aqueous mixture was extracted with ether
  4. washThe ether extracts were washed with water
  5. dry with materialdried over anhydrous magnesium sulphate
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-2a5118fbc91d4390ba2a035d49128c66
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05098929

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