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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Dimethyl Carbonate → Methyl 4,4-dimethyl-2-oxocyclohexane-1-carboxylate

HRID 1619392
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HRID 1619392 반응식
[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][CH2:5][C:4](=[O:8])[CH2:3]1.[H-].[Na+].[C:12](=O)([O:15]C)[O:13][CH3:14]>C1(C)C=CC=CC=1>[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][CH:5]([C:12]([O:13][CH3:14])=[O:15])[C:4](=[O:8])[CH2:3]1
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참가 물질

5

반응물 3

HCID 12021Dimethyl CarbonateHCID 24758Sodium hydrideHCID 76322Cyclohexanone, 3,3-dimethyl-

생성물 1

HCID 5314361Methyl 4,4-dimethyl-2-oxocyclohexane-1-carboxylate

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A solution of 3,3-dimethylcyclohexanone (0.5 g, 3.97 mmol, 1 equiv) and sodium hydride in toluene was stirred at rt for half an hour. To the mixture was added dimethyl carbonate and heated at reflux for 5 h. After the reaction was cooled to rt, the reaction mixture was quenched with water and extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with brine and dried over anhydrous sodium sulfate, then concentrated under reduced pressure to give the crude product, which was directly used for the next step.

후처리

  1. temperatureheated
  2. temperatureat reflux for 5 h
  3. customthe reaction mixture was quenched with water
  4. extractionextracted with ethyl acetate (3×50 mL)
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0d546ada348d4a088d8cbc1313ab3dab
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772301B2

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