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

1,1-Dichloroethane → HCID 19759896, Verbindung

HRID 1586858
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1586858
C(N1C=CN=C1)([N:3]1C=CN=C1)=O.[CH3:13][C:14]1([C:24]([OH:26])=O)[S:21](=[O:23])(=[O:22])[C:17]2[S:18][CH:19]=[CH:20][C:16]=2[CH2:15]1.ClC(Cl)C>>[CH3:13][C:14]1([C:24]([NH2:3])=[O:26])[S:21](=[O:23])(=[O:22])[C:17]2[S:18][CH:19]=[CH:20][C:16]=2[CH2:15]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 63651,1-DichloroethaneHCID 682631,1'-CarbonyldiimidazoleHCID 19759891HCID 19759891, Verbindung

Produkt 1

HCID 19759896HCID 19759896, VerbindungAusbeute 53 %

Versuchsvorschrift

Carbonyldiimidazole (13.3 g, 82.0 mmol) was added to a solution of 2,3-dihydro-2-methylthieno[2,3-b]thiophene-2-carboxylic acid-1,1-dioxide (12.7 g, 54.7 mmol) in dry, degassed DMF (200 mL). The reaction was stirred under N2 until an aliquot quenched with methanol showed no more starting material by tlc (about 1 h). An excess of a saturated solution of NH3 (g) in CHCl3 was added and the reaction stirred 1.5 h. The reaction was diluted with water and extracted with ethyl acetate 3X. The combined organic extracts were washed with brine and dried over MgSO4, filtered, and the solvent removed in vacuo to give a semi-solid. This semi-solid was treated with dichloroethane, cooled in the freezer, and filtered to give the title compound (6.69 g, 53%). 1H NMR (300 MHz,DMSO-d6) 1.70(s,3H), 3.00(d, 1H), 3.85(d,1H), 7.10(d,1H), 7.63(bs,1H exch.), 7.69(bs,1 H, exch.), 8.05(d,1H).

Aufarbeitung

  1. customin dry
  2. customdegassed DMF (200 mL)
  3. customquenched with methanol
  4. customby tlc (about 1 h)
  5. additionAn excess of a saturated solution of NH3 (g) in CHCl3 was added
  6. stirringthe reaction stirred 1.5 h
  7. additionThe reaction was diluted with water
  8. extractionextracted with ethyl acetate 3X
  9. washThe combined organic extracts were washed with brine
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. customthe solvent removed in vacuo
  13. customto give a semi-solid
  14. temperaturecooled in the freezer
  15. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-99982dc7e9544bea8f188a917756e925
Quelldatensatz
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05216020

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion