Sulfuric Acid → 2-Iodo-1-methoxy-4-nitrobenzene

HRID 541571

Reaktionsgleichung

Reaktionsgleichung von HRID 541571
[CH3:1][O:2][C:3]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][C:4]=1N.S(=O)(=O)(O)O.N([O-])=O.[Na+].[I-:22].[K+]>O>[I:22][C:4]1[CH:6]=[C:7]([N+:10]([O-:12])=[O:11])[CH:8]=[CH:9][C:3]=1[O:2][CH3:1]

Komponenten

6

Edukt 4

HCID 1118Sulfuric AcidHCID 4875Potassium IodideHCID 74472-Methoxy-5-nitroanilineHCID 23668193Sodium Nitrite

Produkt 1

HCID 948062-Iodo-1-methoxy-4-nitrobenzeneAusbeute 81,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

2-Methoxy-5-nitroaniline (10.0 g, 0.060 mol) was stirred in water (150 mL) and concentrated (conc.) sulfuric acid (12 mL, 0.22 mol). The solution was cooled below 5° C. with an ice-salt bath, and a solution of sodium nitrite (4.8 g, 0.070 mol) in water (40 mL) was added dropwise while maintaining the temperature below 5° C. A solution of potassium iodide (16.8 g, 0.101 mol) was added and the mixture was heated to 90° C. for 1 hour. Cooling to 0° C. gave dark red crystals which were filtered, washed with water, and dried. Purification by silica gel chromatography using ethyl acetate/hexanes gave the desired compound (13.6 g, 75%). 1H NMR (300 MHz, DMSO-d6): δ 8.57 (s, 1H), 8.28 (d, 1H), 7.19 (d, 1H), 3.98 (s, 3H). LCMS for C7H7INO3 (M+H)+: m/z=280.1.

Aufarbeitung

  1. temperatureThe solution was cooled below 5° C. with an ice-salt bath
  2. temperaturewhile maintaining the temperature below 5° C
  3. temperatureCooling to 0° C.
  4. customgave dark red crystals which
  5. filtrationwere filtered
  6. washwashed with water
  7. customdried
  8. customPurification by silica gel chromatography

Quellen und Nachweise

ORD-Eintrag
ord-691e11ff876a4505b828e13619da3809
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08871753B2

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