Sodium Hydroxide → HCID 178467356, Verbindung

HRID 885424

Reaktionsgleichung

Reaktionsgleichung von HRID 885424
[Cl:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-])=O)[C:3]=1[NH2:4].[OH-].[Na+].[CH2:14]([O:16][C:17](OCC)(OCC)OCC)[CH3:15]>C(O)C>[Cl:1][C:2]1[C:3]2[NH:4][C:17]([O:16][CH2:14][CH3:15])=[N:9][C:5]=2[CH:6]=[CH:7][CH:8]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
130 °C

Versuchsvorschrift

2-Chloro-6-nitroaniline (3.45 g, 20.0 mmol) and stannous chloride dihydrate (18.05 g, 80.0 mmol) were heated under reflux in ethanol (80 mL) for 3 hr. The reaction mixture was neutralized with aqueous sodium hydroxide solution, and the precipitate was filtered off. The filtrate was extracted with ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was mixed with tetraethoxymethane (10 mL, 47.7 mmol) and the mixture was stirred at 130° C. for 12 hr. The reaction mixture was purified by silica gel column chromatography (hexane/ethyl acetate=50/50) to give the title compound (1.38 g, 35%).

Aufarbeitung

  1. filtrationthe precipitate was filtered off
  2. extractionThe filtrate was extracted with ethyl acetate
  3. washwashed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe reaction mixture was purified by silica gel column chromatography (hexane/ethyl acetate=50/50)

Quellen und Nachweise

ORD-Eintrag
ord-6e1933e1b30e41918fc506baf6325c5e
Quelldatensatz
uspto-grants-2012_08
Patentnummer
US08242151B2

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