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Hydrochloric Acid → 3,5-Dinitrobenzoyl chloride

HRID 380719
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 380719
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([N+:13]([O-:15])=[O:14])[CH:12]=1)[C:7](O)=[O:8])([O-:3])=[O:2].S(Cl)([Cl:18])=O.[N+](C1C([N+]([O-])=O)=C(C=CC=1)C(O)=O)([O-])=O.Cl>CN(C=O)C.C(OCC)(=O)C>[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[C:11]([N+:13]([O-:15])=[O:14])[CH:12]=1)[C:7]([Cl:18])=[O:8])([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 74333,5-Dinitrobenzoic acidHCID 24386Thionyl ChlorideHCID 2833272,3-Dinitrobenzoic acid

Produkt 1

HCID 74323,5-Dinitrobenzoyl chlorideAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228
Dimethylformamide
Lösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

3,5 dinitrobenzoic acid and ethyl acetate were placed in a reaction vessel. While thionyl chloride with some drops of DMF (about double as many moles as dinitrobenzoic acid) was dropped into the reaction mixtures, the reaction mixtures were refluxed with stirring until the generation of hydrogen chloride gas stopped. The reacted solution was concentrated until a solid could be precipitated and was poured into hexane and then the precipitated solid was separated by filtration. 3,5-dinitrobenzoic chloride was obtained in a 90% yield.

Aufarbeitung

  1. customthe reaction mixtures
  2. temperaturewere refluxed
  3. concentrationThe reacted solution was concentrated until a solid
  4. customcould be precipitated
  5. additionwas poured into hexane
  6. customthe precipitated solid was separated by filtration

Quellen und Nachweise

ORD-Eintrag
ord-94448e8b87084c39ae84e619c07fa7d8
Quelldatensatz
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06303742B1

Notizen zur Reaktion

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