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Nitric Acid → 1-Bromo-4-fluoro-2-methyl-5-nitrobenzene

HRID 400553
Notes
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Reaction equation

HRID 400553 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH3:9].[N+:10]([O-])([OH:12])=[O:11]>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:5]([F:8])=[CH:4][C:3]=1[CH3:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 944Nitric AcidHCID 967432-Bromo-5-fluorotoluene

Product 1

HCID 100369831-Bromo-4-fluoro-2-methyl-5-nitrobenzeneYield 104.8%

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

Combine 1-bromo-4-fluoro-2-methylbenzene (30.0 g, 159 mmol) in concentrated sulfuric acid (100 mL), cool to about −5° C., and treat dropwise with nitric acid (11.00 mL, 174 mmol) over 20 minutes. Allow reaction mixture to warm to RT and stir for 30 min. Pour onto crushed ice with stiffing and partition with tert-butyl methyl ether (MTBE) (200 mL). Separate the aqueous layer and extract with MTBE (2×50 mL). Combine organic layers, dry and concentrate under reduced pressure to provide 1-bromo-4-fluoro-2-methyl-5-nitrobenzene as an orange-colored viscous oil (39.0 g).

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. customAllow reaction mixture
  2. additionPour
  3. customonto crushed ice with stiffing
  4. custompartition with tert-butyl methyl ether (MTBE) (200 mL)
  5. customSeparate the aqueous layer
  6. extractionextract with MTBE (2×50 mL)
  7. customCombine organic layers, dry
  8. concentrationconcentrate under reduced pressure

Sources & evidence

ORD record
ord-11409640bb6745f38880db83dafaac01
Source dataset
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08741911B2

Reaction notes

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