tert-Butanol → Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoate

HRID 494345

Reaktionsgleichung

Reaktionsgleichung von HRID 494345
C([C:4]1[C:13]([N+:14]([O-:16])=[O:15])=[CH:12][CH:11]=[CH:10][C:5]=1[C:6]([O:8][CH3:9])=[O:7])(O)=O.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:24])C=CC=CC=1.C([N:36]([CH2:39]C)CC)C.[C:41]([OH:45])([CH3:44])([CH3:43])[CH3:42]>CN(C=O)C>[C:41]([O:45][C:39]([NH:36][C:4]1[C:13]([N+:14]([O-:16])=[O:15])=[CH:12][CH:11]=[CH:10][C:5]=1[C:6]([O:8][CH3:9])=[O:7])=[O:24])([CH3:44])([CH3:43])[CH3:42]

Komponenten

6

Edukt 4

HCID 6386tert-ButanolHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 43994772-(Methoxycarbonyl)-6-nitrobenzoic acid

Produkt 1

HCID 9965968Methyl 2-((tert-butoxycarbonyl)amino)-3-nitrobenzoateAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of methyl 2-carboxy-3-nitrobenzoate (7.23 g) in DMF (50 ml) was added diphenylphosphoryl azide (11.3 g) at room temperature and then triethylamine (6.7 ml) was added dropwise to the stirred reaction mixture. After stirring at room temperature for 3 hours, tert-butanol (54 ml) was added to the stirred reaction mixture. After stirring at room temperature for 30 min., the reaction mixture was gradually warmed, then heated under reflux for 1 hour and evaporated to dryness. The resultant residue was dissolved in ethyl acetate, washed with dilute hydrochloric acid, aqueous sodium bicarbonate, and water, and then dried. After evaporation of the solvent, methanol was added to the resultant residue and the mixture was cooled to give colorless crystals (6.7 g, 70%).

Aufarbeitung

  1. stirringAfter stirring at room temperature for 30 min.
  2. temperaturethe reaction mixture was gradually warmed
  3. temperatureheated
  4. temperatureunder reflux for 1 hour
  5. customevaporated to dryness
  6. dissolutionThe resultant residue was dissolved in ethyl acetate
  7. washwashed with dilute hydrochloric acid, aqueous sodium bicarbonate, and water
  8. customdried
  9. customAfter evaporation of the solvent, methanol
  10. additionwas added to the resultant residue
  11. temperaturethe mixture was cooled

Quellen und Nachweise

ORD-Eintrag
ord-a8992be35f9f44978c6cb19255a28a84
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07538133B2

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