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Hydrochloric Acid → 2-Iodo-3-nitrobenzoic acid

HRID 1639831
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1639831
C(N[C:5]1[C:14]([N+:15]([O-:17])=[O:16])=[CH:13][CH:12]=[CH:11][C:6]=1[C:7]([O:9]C)=[O:8])(=O)C.[OH-].[K+].Cl.N([O-])=O.[Na+].[I-:25].[K+].II>O.CS(C)=O>[I:25][C:5]1[C:14]([N+:15]([O-:17])=[O:16])=[CH:13][CH:12]=[CH:11][C:6]=1[C:7]([OH:9])=[O:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 6

HCID 313Hydrochloric AcidHCID 807IodineHCID 4875Potassium IodideHCID 14797Potassium HydroxideHCID 2782278Methyl 2-acetamido-3-nitrobenzoateHCID 23668193Sodium Nitrite

Produkt 1

HCID 220966
2-Iodo-3-nitrobenzoic acid
Ausbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 679Dimethyl SulfoxideLösungsmittelHCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A mixture of methyl 2-(acetylamino)-3-nitrobenzoate (4.19 g, 17.6 mmol) and potassium hydroxide (4.93 g, 88.0 mmol) in water (20 mL) was stirred at 60° C. overnight. The resulting solid was collected by filtration, washed with methanol, and is suspended in water (14 mL). Concentrated hydrochloric acid (7.3 mL, 88 mmol) was added to the suspension, and a solution of sodium nitrite (1.88 g, 27.3 mmol) in water (10 mL) was added at 0° C. over 1.5 hr. The reaction mixture was added to a solution of potassium iodide (4.53 g, 27.3 mmol) and iodine (3.73 g, 14.7 mmol) in dimethyl sulfoxide (130 mL) at 5° C. over 20 min. The resulting reaction mixture was stirred at 50° C. for 20 min, and extracted with ethyl acetate. The extract was washed with water, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with hexane to give the title compound (3.71 g, yield 72%).

Aufarbeitung

  1. filtrationThe resulting solid was collected by filtration
  2. washwashed with methanol
  3. customThe resulting reaction mixture
  4. stirringwas stirred at 50° C. for 20 min
  5. extractionextracted with ethyl acetate
  6. washThe extract was washed with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure
  9. washThe residue was washed with hexane

Quellen und Nachweise

ORD-Eintrag
ord-0783df7c8fab4e3980b65a77e067d3ac
Quelldatensatz
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08110585B2

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