StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Ethyl butyrate → 5-Ethyl-2-thiouracil

HRID 705851
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 705851
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]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

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

Produkt 1

HCID 30020425-Ethyl-2-thiouracilAusbeute 82 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 176Acetic Acid
Lösungsmittel
HCID 962WaterLösungsmittel
HCID 3283Diethyl EtherLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-267e12404e0a49179f013a737b5f339a
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09174968B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion