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Sulfuric Acid → Ethyl 4-methyl-3-(thiophen-2-yl)isoxazole-5-carboxylate

HRID 2388188
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HRID 2388188 반응식
O[N:2]=[C:3]([C:13]1[S:14][CH:15]=[CH:16][CH:17]=1)[CH:4]([CH3:12])[C:5](=[O:11])[C:6]([O:8][CH2:9][CH3:10])=[O:7].S(=O)(=O)(O)O.C(=O)(O)[O-].[Na+]>C(O)C>[CH3:12][C:4]1[C:3]([C:13]2[S:14][CH:15]=[CH:16][CH:17]=2)=[N:2][O:11][C:5]=1[C:6]([O:8][CH2:9][CH3:10])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 516892Sodium BicarbonateHCID 86648118Ethyl 4-(hydroxyimino)-3-methyl-2-oxo-4-(thiophen-2-yl)butanoate

생성물 1

HCID 67530636Ethyl 4-methyl-3-(thiophen-2-yl)isoxazole-5-carboxylate수율 54.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 4-(hydroxyimino)-3-methyl-2-oxo-4-(thiophen-2-yl)butanoate (7.7 g, 30.2 mmol) and concentrated sulfuric acid (8 mL) were added to 120 mL of absolute ethanol and the mixture was refluxed for 20 hours. After the mixture cooled to room temperature, saturated sodium bicarbonate solution was added to neutralize the mixture. The product was extracted with EtOAc and the combined organic layer was dried over MgSO4 and concentrated to give 3.9 g of the title compound. MS: (+) m/z 238.38 (M+1).

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후처리

  1. temperaturethe mixture was refluxed for 20 hours
  2. extractionThe product was extracted with EtOAc
  3. dry with materialthe combined organic layer was dried over MgSO4
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-7ceb9cda32c54a849d60343ae2970238
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08269008B2

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