Nitric Acid → HCID 59560629, compound

HRID 1176696Notes

Reaction equation

HRID 1176696 reaction equation
C[O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[C:7](F)=[CH:6][C:5]=1[Br:14].O[S:17](O)(=O)=O.[N+]([O-])(O)=O.C[O:26][C:27](=O)[C:28]1C=CC(F)=CC=1Br.[OH-].[Na+]>CCOC(C)=O>[Br:14][C:5]1[C:4]([C:3]([OH:2])=[O:15])=[CH:9][C:8]2[NH:10][C:27](=[O:26])[CH2:28][S:17][C:7]=2[CH:6]=1

Participants

7

Reactant 5

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 7210837Methyl 2-bromo-4-fluorobenzoateHCID 43449031Benzoic acid, 2-bromo-4-fluoro-5-nitro-, methyl ester

Product 1

HCID 59560629HCID 59560629, compoundYield 43%

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

2-Bromo-4-fluoro-5-nitro-benzoic acid methyl ester. To conc. fuming H2SO4 (8 mL) at 0° C. was added conc. fuming HNO3 (8 mL) and the mixture allowed to stand for 5 min. To a solution of 2-bromo-4-fluoro-benzoic acid methyl ester (9.32 g, 40 mmol) at 0° C., the mixture of acids was added dropwise over 30 min. The mixture was allowed to warm to RT and was stirred for 18 h. The mixture was poured into ice water, diluted with EtOAc, and treated with 6 N NaOH. The aqueous layer was extracted with EtOAc (3×300 mL). The combined organic layers were washed with brine (200 mL), dried (MgSO4), and concentrated. The crude material was purified on SiO2 (0-25% EtOAc/hexanes) to provide 4.9 g (43%) of the title compound. 1H NMR (500 MHz, CDCl3): 8.61 (d, J=8.0, 1H), 7.66 (d, J=10.0, 1H), 3.91 (s, 3H).

Workup

  1. additionwas added dropwise over 30 min
  2. extractionThe aqueous layer was extracted with EtOAc (3×300 mL)
  3. washThe combined organic layers were washed with brine (200 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. customThe crude material was purified on SiO2 (0-25% EtOAc/hexanes)

Sources & evidence

ORD record
ord-061d55f98d4e464184d78ed34b653b86
Source dataset
uspto-grants-2010_11
Patent number
US07842810B2

Reaction notes

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