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Sodium Hydroxide → 3,5-Diaminobenzonitrile

HRID 1190897
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1190897
[N+:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([N+:12]([O-])=O)[CH:11]=1)[C:7]#[N:8])([O-])=O.Cl[Sn]Cl.[OH-].[Na+]>Cl>[NH2:1][C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([NH2:12])[CH:11]=1)[C:7]#[N:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 200623,5-DinitrobenzonitrileHCID 24479Stannous Chloride

Produkt 1

HCID 128973293,5-DiaminobenzonitrileAusbeute 57 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

To 3,5-dinitrobenzonitrile (5.0 g, 25.89 mmol) in 20 mL of HCl 1M, was added SnCl2 (34.4 g, 7 eq). The reaction mixture was stirred at room temperature for 2 h and then cooled to 0° C. The mixture was made alkaline with a 50% aqueous solution of NaOH and the precipitate was removed by filtration. The filtrate was extracted with ethyl acetate and the combined organic layers were evaporated. The residue and the precipitate were purified by flash chromatography on silica gel (DCM/MeOH//95/5) to yield expected compound as an orange solid (1.95 g, 57% yield). m/z (ESI) 134.0 [M+H]+.

Aufarbeitung

  1. temperaturecooled to 0° C
  2. customthe precipitate was removed by filtration
  3. extractionThe filtrate was extracted with ethyl acetate
  4. customthe combined organic layers were evaporated
  5. customThe residue and the precipitate were purified by flash chromatography on silica gel (DCM/MeOH//95/5)

Quellen und Nachweise

ORD-Eintrag
ord-c9d06e2ce5ab4de282e6822838a95cc4
Quelldatensatz
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08680095B2

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