Dimethylformamide → 1,2-Benzenedicarboxylic acid, 3-nitro-, 1,2-dimethyl ester

HRID 448309

Reaktionsgleichung

Reaktionsgleichung von HRID 448309
[CH3:1]I.[N+:3]([C:6]1[CH:14]=[CH:13][CH:12]=[C:8](C(O)=O)[C:7]=1[C:15]([OH:17])=[O:16])([O-:5])=[O:4].[C:18](=[O:21])(O)[O-].[Na+].CN([CH:26]=[O:27])C>>[CH3:18][O:21][C:26](=[O:27])[C:8]1[C:7](=[C:6]([N+:3]([O-:5])=[O:4])[CH:14]=[CH:13][CH:12]=1)[C:15]([O:17][CH3:1])=[O:16]

Komponenten

5

Edukt 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 690433-Nitrophthalic acidHCID 516892Sodium Bicarbonate

Produkt 1

HCID 2499121,2-Benzenedicarboxylic acid, 3-nitro-, 1,2-dimethyl esterAusbeute 95 %

Versuchsvorschrift

Methyl iodide (30.2 g, 213 mmol) was added to a stirred mixture of 3-nitrophthalic acid (15.0 g, 71.0 mmol) and sodium bicarbonate (23.9 g, 284 mmol) in DMF (150 mL) at room temperature, and the mixture was then heated in an oil bath set to 60° C. for 4 hours. The mixture was then poured into 700 mL of ice water. After the ice melted, the mixture was extracted with ethyl acetate (3×150 mL) and the organic phases were washed with water (7×500 mL), dried (MgSO4) and evaporated, providing 16.2 g of the product as a pale yellow solid in 95% yield: 1H NMR (CDCl3) δ 3.95 (s, 3H), 4.02 (s, 3H), 7.69 (t, J=8.1 Hz, 1H), 8.36 (m, 2H).

Aufarbeitung

  1. temperaturethe mixture was then heated in an oil bath
  2. extractionthe mixture was extracted with ethyl acetate (3×150 mL)
  3. washthe organic phases were washed with water (7×500 mL)
  4. dry with materialdried (MgSO4)
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-ac9a3893add44d259c81f253b54b18fe
Quelldatensatz
uspto-grants-2013_07
Patentnummer
US08481568B2

Verknüpfte Notizen

Wird geladen…