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Ethyl butyrate → 5-Ethyl-2-thiouracil

HRID 705851
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HRID 705851 반응식
CC(C)([O-])C.[K+].[C:7]([O:12]CC)(=O)[CH2:8][CH2:9][CH3:10].[CH:15](OCC)=O.[NH2:20][C:21]([NH2:23])=[S:22]>C1COCC1.C(OCC)C.O.CC(O)=O>[CH2:9]([C:8]1[C:7](=[O:12])[NH:20][C:21](=[S:22])[NH:23][CH:15]=1)[CH3:10]
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참가 물질

9

반응물 4

HCID 7762Ethyl butyrateHCID 8025Ethyl formateHCID 2723790ThioureaHCID 23665647Potassium tert-butoxide

생성물 1

HCID 30020425-Ethyl-2-thiouracil수율 82%

시약·촉매·용매 4

HCID 176Acetic Acid용매
HCID 962
Water
용매
HCID 3283Diethyl Ether용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a suspension of potassium tert-butoxide (12.08 g, 108 mmol) in THF (40 mL) was added a solution of ethyl butyrate (5.69 mL, 43.0 mmol) and ethyl formate (6.93 mL, 86 mmol) in diethyl ether (40.0 mL) dropwise under nitrogen. The mixture was stirred at room temperature for 3 h. After removing the solvent, the residue oil was dissolved in isopropanol (350 mL), and thiourea (6.55 g, 86 mmol) was added. The mixture was stirred at reflux overnight, and then concentrated in vacuo to get a solid. The solid was dissolved in water, adjusted pH to 4 with AcOH, and extracted by DCM. The organic layer was dried over Na2SO4, filtered and concentrated to afford the title compound (5.5 g, 82% yield) as a pink solid.

후처리

  1. customAfter removing the solvent
  2. dissolutionthe residue oil was dissolved in isopropanol (350 mL)
  3. stirringThe mixture was stirred
  4. temperatureat reflux overnight
  5. concentrationconcentrated in vacuo
  6. customto get a solid
  7. extractionextracted by DCM
  8. dry with materialThe organic layer was dried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-267e12404e0a49179f013a737b5f339a
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174968B2

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