Hydrochloric Acid → 4,6-Dinitroresorcinol

HRID 2211334

Reaktionsgleichung

Reaktionsgleichung von HRID 2211334
C[O:2][C:3]1[C:4]([N+:13]([O-:15])=[O:14])=[CH:5][C:6]([N+:10]([O-:12])=[O:11])=[C:7]([OH:9])[CH:8]=1.CN(C)C=O.Cl.Cl>CN(C)C=O>[N+:10]([C:6]1[CH:5]=[C:4]([N+:13]([O-:15])=[O:14])[C:3]([OH:2])=[CH:8][C:7]=1[OH:9])([O-:12])=[O:11]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 2667955-Methoxy-2,4-dinitrophenol2×HCID 10920465N,N-dimethylformamide;hydrochloride

Produkt 1

HCID 611584,6-DinitroresorcinolAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
130 °C

Versuchsvorschrift

To a 100 mL round-bottom flask is added 2.14 g (10 mmol) of 5-methoxy-2,4-dinitrophenol (MDNP) and 1.31 g (12 mmol) of DMF-HCl in 30 mL of N,N-dimethylformamide (DMF). This mixture is stirred at 130° C. and monitored by High Pressure Liquid Chromatography (HPLC). After 8.5 hours essentially no MDNP is observed by HPLC. The reaction mixture is poured into 100 mL of 1N HCl, and extracted with ethyl acetate (EtOAc, 3×30 mL). The combined organics are washed with a single portion of 0.1N HCl, dried (Na2SO4) and concentrated by rotary evaporation to give crude 4,6-dinitroresorcinol (DNR) as a yellow solid (1.9 g, 95% yield): melting point (m.p.) 205° C. to 210° C., 1H NMR (CDCl3)δ11.03 (s,2H), 9.08 (s,1H), 6.82 (s,1H).

Aufarbeitung

  1. extractionextracted with ethyl acetate (EtOAc, 3×30 mL)
  2. washThe combined organics are washed with a single portion of 0.1N HCl
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated by rotary evaporation

Quellen und Nachweise

ORD-Eintrag
ord-764ba658150c4f60b7e970e197d8ecff
Quelldatensatz
uspto-grants-1995_10
Patentnummer
US05463129

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