Water → 4-(2-Furyl)Aniline Hydrochloride

HRID 2086642Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2086642
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[O:11][CH:12]=[CH:13][CH:14]=2)=[CH:6][CH:5]=1)([O-])=O.O>C(O)C>[O:11]1[CH:12]=[CH:13][CH:14]=[C:10]1[C:7]1[CH:8]=[CH:9][C:4]([NH2:1])=[CH:5][CH:6]=1

Komponenten

4

Edukt 2

HCID 962WaterHCID 6049692-(4-Nitrophenyl)furan

Produkt 1

HCID 41911054-(2-Furyl)Aniline Hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

To a suspension of 2-(4-nitrophenyl)furan (0.378 g, 2 mmol, prepared according to the method of Heterocycles, 1990, 31, 1951) in ethanol (20 mL) was heated to 70° C. and added stannous chloride dihydrate (2.26 g, 10 mmol) and the mixture was stirred for 2 hours. The reaction mixture was cooled to room temperature and poured into water (50 mL), the whole was extracted with ethyl acetate (30 mL×2). The organic layer was dried over Na2SO4, filtered through celite and concentrated to give the crude subtitle compound (0.35 g).

Aufarbeitung

  1. customprepared
  2. temperatureThe reaction mixture was cooled to room temperature
  3. extractionthe whole was extracted with ethyl acetate (30 mL×2)
  4. dry with materialThe organic layer was dried over Na2SO4
  5. filtrationfiltered through celite and
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-16dc3cc55f8545efb3dd89f408ea84ea
Quelldatensatz
uspto-grants-2004_04
Patentnummer
US06727238B2

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