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Diethyl Ether → 4-Nitro-o-toluic acid

HRID 553355
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 553355
I[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:11].[C:12](=O)([O-:14])[O-:13].[K+].[K+].C(OCC)C.CCCCCC>O.CN(C)C=O.C(OCC)(=O)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd](Cl)Cl>[N+:8]([C:7]1[CH:6]=[CH:5][C:4]([C:12]([OH:14])=[O:13])=[C:3]([CH3:11])[CH:2]=1)([O-:10])=[O:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 3283Diethyl EtherHCID 8058HexaneHCID 11430Potassium CarbonateHCID 2347812-Iodo-3-nitrotoluene

Produkt 1

HCID 747904-Nitro-o-toluic acidAusbeute 31,2 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 6102075
Dichlorobis(triphenylphosphine)palladium
Katalysator
HCID 962WaterLösungsmittel2×
HCID 6228DimethylformamideLösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A mixture of 1.0 g (3.8 mmol) of 2-iodo-nitrotoluene, 2.1 g (15.2 mmol) potassium carbonate and 27 mg (0.038 mmol) of palladium(II) dichloride bis(triphenylphosphine) in a mixture of 5 mL of water and 10 mL of N,N-dimethylformamide. This was placed in a Fisher/Porter bottle under 15 psig of carbon monoxideand heated at 70° C. for 16 hours. The solution became homogeneous when heated. The reaction was cooled, diethyl ether and water was added, the organic layer separated and discarded. The aqueous layer was acidified with IN hydrohloric acid, extracted with ethyl acetate, washed with water, brine, dried over magnesium sulfate, filtered and concentrated to yield 0.5 g of crude material. This dissolved in ethyl acetate, hexane added and the resulting brown solid discarded. The filtrate was concentrated, and then recrystallized fom diethyl ether/hexane to afford 215 mg of 4-nitro-2-methylbenzoic acid, m/e=182 (M+H).

Aufarbeitung

  1. temperatureheated
  2. temperatureThe reaction was cooled
  3. customthe organic layer separated
  4. extractionextracted with ethyl acetate
  5. washwashed with water, brine
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto yield 0.5 g of crude material
  10. concentrationThe filtrate was concentrated
  11. customrecrystallized fom diethyl ether/hexane

Quellen und Nachweise

ORD-Eintrag
ord-2e69f8efd29f484b93949c4b6aa97162
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
USRE042889E1

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