Nitric Acid → 4,5-Difluoro-2-nitrobenzoic acid

HRID 359966Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 359966
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5]([OH:7])=[O:6].CCCC(O[C@@]1(C(COC(C)=O)=O)[C@@]2(C)C[C@H](O)[C@]3(F)[C@]4(C)C(=CC(C=C4)=O)[C@@H](F)C[C@H]3[C@@H]2CC1)=O.[N+:48]([O-])([OH:50])=[O:49]>S(=O)(=O)(O)O>[N+:48]([C:8]1[CH:9]=[C:10]([F:11])[C:2]([F:1])=[CH:3][C:4]=1[C:5]([OH:7])=[O:6])([O-:50])=[O:49]

Komponenten

5

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Into 100 mL of 96% sulfuric acid was placed 3,4-difluorobenzoic acid(11.95 g, 0.0756 mol). The solution was stirred at room temperature until the DFBA was dissolved, and then cooled to 0° C. Nitric acid (7.9 g of 90% fuming) was added dropwise to the cooled mixture. After addition, the solution was warmed to room temperature and stirred until completion of the reaction. After drying, 11.88 g of 2-nitro-4,5-difluorobenzoic acid was isolated. The material was identified by GCMS and 19F NMR analysis. An additional 2.41 g of product was obtained by extraction of the acid washes and removal of the solvent.

Aufarbeitung

  1. dissolutionwas dissolved
  2. additionAfter addition
  3. temperaturethe solution was warmed to room temperature
  4. customAfter drying

Quellen und Nachweise

ORD-Eintrag
ord-c48e92e255584abb9fa0110bf70f4c79
Quelldatensatz
uspto-grants-1991_03
Patentnummer
US05003103

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