Hydrochloric Acid → HCID 22494951, Verbindung

HRID 1816542Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1816542
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([N+:13]([O-:15])=[O:14])[CH:4]=1)#[N:2].CO.[ClH:18]>C1COCC1>[Cl-:18].[N+:13]([C:5]1[CH:4]=[C:3]([CH:12]=[CH:11][C:6]=1[C:7]([O:9][CH3:10])=[O:8])[CH2:1][NH3+:2])([O-:15])=[O:14]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 11356202Methyl 4-cyano-2-nitrobenzoate

Produkt 1

HCID 22494951HCID 22494951, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

700 ml of a 1 M BH3 solution in THF (0.7 mol) are metered in the course of one hour at 40-50° C. into a solution of 144 g (0.7 mol) of methyl 4-cyano-2-nitrobenzoate in 250 ml of THF and the mixture is subsequently refluxed for a further. 1.5 hours. The reaction mixture is then treated with 600 ml of methanol saturated with hydrogen chloride gas, with ice-cooling, and refluxed for one hour. The mixture is concentrated completely under atmospheric pressure and reevaporated with 700 ml of methanol. The residue which remains is stirred with 500 ml of ethyl acetate and filtered, and the product is dried. This gives 115 g (67%) of 3-nitro-4-methoxycarbonylbenzyl-ammonium chloride of melting point 247-248° C.

Aufarbeitung

  1. temperaturethe mixture is subsequently refluxed for a further
  2. custom1.5 hours
  3. temperaturecooling
  4. temperaturerefluxed for one hour
  5. concentrationThe mixture is concentrated completely under atmospheric pressure
  6. customreevaporated with 700 ml of methanol
  7. filtrationfiltered
  8. customthe product is dried

Quellen und Nachweise

ORD-Eintrag
ord-c7ed7674432142b3a285d25ae2f909aa
Quelldatensatz
uspto-grants-2005_04
Patentnummer
US06884903B2

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