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1,3-Diiodo-5-nitrobenzene → 3,5-DIIODOANILINE

HRID 486835
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 486835
[I:1][C:2]1[CH:3]=[C:4]([N+:9]([O-])=O)[CH:5]=[C:6]([I:8])[CH:7]=1>C(O)C>[I:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:6]([I:8])[CH:7]=1)[NH2:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 121342561,3-Diiodo-5-nitrobenzene

Produkt 1

HCID 121342543,5-DIIODOANILINEAusbeute 61,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A mixture of 61.5 g (0.164M) of 3,5-diiodonitrobenzene and 111.1 g (0.4924M) of stannous chloride in 900 mL of ethanol was heated to reflux 1.5 hrs under nitrogen. The reaction mixture was cooled and most of the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and excess ice-cold 5N sodium hydroxide and ice. The organic phase was separated, washed with sat'd sodium chloride solution, and dried over anhyd. magnesium sulfate. Solvent removal afforded a crude oil which was purified on silica gel using 8:1:1 mixture of hexane:methylene chloride:ethyl acetate to give 35 g of 3,5-diiodoaniline as a light tan colored solid.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureto reflux 1.5 hrs under nitrogen
  3. temperatureThe reaction mixture was cooled and most of the solvent
  4. customwas removed in vacuo
  5. customThe residue was partitioned between ethyl acetate and excess ice-cold 5N sodium hydroxide and ice
  6. customThe organic phase was separated
  7. washwashed with sat'd sodium chloride solution
  8. customdried over anhyd
  9. customSolvent removal
  10. customafforded a crude oil which
  11. customwas purified on silica gel using 8:1:1 mixture of hexane

Quellen und Nachweise

ORD-Eintrag
ord-410acc0ad4a048879d6105580d543ac9
Quelldatensatz
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05292879

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