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Nitric Acid → 5-Fluoro-2-methyl-1,3-dinitrobenzene

HRID 1416904
Notes
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Reaction equation

HRID 1416904 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[N+:12]([C:6]1[CH:7]=[C:2]([F:1])[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[C:5]=1[CH3:8])([O-:14])=[O:13]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 944Nitric AcidHCID 679654-Fluoro-2-nitrotoluene

Product 1

HCID 184653725-Fluoro-2-methyl-1,3-dinitrobenzene

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent2×

Conditions

Temperature
2.5 °C

Procedure

Fuming sulfuric acid (180 mL) is added dropwise to 4-fluoro-2-nitrotoluene (50.21 g) under an argon atmosphere. The internal temperature of the mixture is maintained at 0-5° C. using an ice/sodium chloride bath. A preformed (ice bath) mixture of fuming nitric acid (30 mL) and fuming sulfuric acid (90 mL) is added dropwise to the previous solution over three hours. The reaction is then allowed to warm to room temperature. After stirring at room temperature for 2 hours, the mixture is poured slowly into ice and the products are extracted with methylene chloride (4×500 mL). The combined extracts are dried over magnesium sulfate, filtered and rotary evaporated. The crude mixture is filtered through a short pad of silica gel, using 10% ethyl acetate/hexanes as solvent, then recrystallized from ethyl acetate/hexanes to afford 2,6-dinitro-4-fluorotoluene as a pale yellow solid.

Workup

  1. additionis added dropwise to the previous solution over three hours
  2. temperatureto warm to room temperature
  3. additionthe mixture is poured slowly into ice
  4. extractionthe products are extracted with methylene chloride (4×500 mL)
  5. dry with materialThe combined extracts are dried over magnesium sulfate
  6. filtrationfiltered
  7. filtrationThe crude mixture is filtered through a short pad of silica gel
  8. customrecrystallized from ethyl acetate/hexanes

Sources & evidence

ORD record
ord-72e04db3eb064587b1ed225eb7ba1cc6
Source dataset
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05916900

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes