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Sodium Hydroxide → Benzoic acid, 2-amino-5-fluoro-3-nitro- (9CI)

HRID 85180
Notes
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Reaction equation

HRID 85180 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([N+:18]([O-:20])=[O:19])[C:5]([NH:11]C(=O)C(F)(F)F)=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].[OH-].[Na+]>C(O)C>[NH2:11][C:5]1[C:4]([N+:18]([O-:20])=[O:19])=[CH:3][C:2]([F:1])=[CH:10][C:6]=1[C:7]([OH:9])=[O:8]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 86653799HCID 86653799, compound

Product 1

HCID 18548624Benzoic acid, 2-amino-5-fluoro-3-nitro- (9CI)Yield 90%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
80 °C

Procedure

To a solution of 5-fluoro-3-nitro-2-(2,2,2-trifluoroacetamido)benzoic acid (141; 1.2 g, 4.1 mmol) in ethanol (20 mL) was added 10% aqueous sodium hydroxide solution (20 mL). The resulting reaction mixture was stirred at 80° C. for 3 h. Upon cooling to room temperature, the reaction mixture was concentrated under reduced pressure. The resulting orange solids were acidified with dilute HCl, filtered and dried to afford 2-amino-5-fluoro-3-nitrobenzoic acid 142 (0.73 g, 90%).

Workup

  1. customThe resulting reaction mixture
  2. temperatureUpon cooling to room temperature
  3. concentrationthe reaction mixture was concentrated under reduced pressure
  4. filtrationfiltered
  5. customdried

Sources & evidence

ORD record
ord-f8e421e2af0e40ad88c6ac557de2ea56
Source dataset
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08846947B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes