Diethyl Ether → Ethyl 5-(4-aminophenylthio)-4-nitrothiophene-2-carboxylate

HRID 605373Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 605373
Cl[C:2]1[S:6][C:5]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([SH:22])=[CH:18][CH:17]=1.C([O-])(=O)C.[Na+].C(OCC)C>C(O)C>[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([S:22][C:2]2[S:6][C:5]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[CH:4][C:3]=2[N+:12]([O-:14])=[O:13])=[CH:18][CH:17]=1

Komponenten

6

Edukt 4

HCID 3283Diethyl EtherHCID 145104-AminothiophenolHCID 517045Sodium AcetateHCID 56763846HCID 56763846, Verbindung

Produkt 1

HCID 67040833Ethyl 5-(4-aminophenylthio)-4-nitrothiophene-2-carboxylateAusbeute 85 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

The product of Example 430A (1.0 g, 4.244 mmol), 4-aminothiophenol (0.797 g, 6.366 mmol), and anhydrous sodium acetate (1.74 g, 21.22 mmol) were heated in anhydrous ethanol (40 mL) under a nitrogen atmosphere at reflux for 30 minutes. The reaction was cooled to room temperature, partitioned with ethyl acetate (100 mL) and water (50 mL), separated layers, and washed organic phase with water (2×50 mL) and brine (50 mL). The organic extract was dried over sodium sulfate, filtered, and concentrated by rotary evaporation. Trituration of the resulting solid with ethyl ether (2×30 mL) afforded the title compound as a bright yellow solid (1.167 g, 3.598 mmol, 85%). 1H NMR (300 MHz, DMSO-D6) δ ppm 1.24 (t, J=7.17 Hz, 3 H) 4.24 (q, J=7.23 Hz, 2 H) 5.94 (s, 2 H) 6.71 (d, J=8.82 Hz, 2 H) 7.35 (d, J=8.46 Hz, 2 H) 8.08 (s, 1 H); MS (ESI+) m/z 325 (M+H)+, MS (ESI−) m/z 323 (M−H)−.

Aufarbeitung

  1. temperatureat reflux for 30 minutes
  2. custompartitioned with ethyl acetate (100 mL) and water (50 mL)
  3. customseparated layers
  4. washwashed organic phase with water (2×50 mL) and brine (50 mL)
  5. extractionThe organic extract
  6. dry with materialwas dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated by rotary evaporation

Quellen und Nachweise

ORD-Eintrag
ord-13a78b58b5a9458c8a37068dcc6a64aa
Quelldatensatz
uspto-grants-2011_03
Patentnummer
US07910595B2

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