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Ethanol → Methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate

HRID 1501702
Notes
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Reaction equation

HRID 1501702 reaction equation
[CH3:1][C:2]1[C:11]([N+:12]([O-])=O)=[CH:10][C:9]([C:15]([F:18])([F:17])[F:16])=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].C(O)C.[NH4+].[Cl-]>[Fe]>[NH2:12][C:11]1[C:2]([CH3:1])=[C:3]([CH:8]=[C:9]([C:15]([F:16])([F:17])[F:18])[CH:10]=1)[C:4]([O:6][CH3:7])=[O:5]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 68295416Methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate

Product 1

HCID 68295733Methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate

Reagents, catalysts & solvents 1

HCID 23925IronCatalyst

Conditions

Temperature
90 °C

Procedure

To a stirred solution of methyl 2-methyl-3-nitro-5-(trifluoromethyl)benzoate (1 equiv.) in ethanol (2 mL per 1 mmol), was added NH4Cl solution (5.1 equiv., dissolved in water. Volume of water equivalent to volume of ethanol) followed by Fe powder (8 equiv.). the resulting reaction mixture was stirred at 90° C. for 1 h. On completion, the reaction mixture was filtered and the filtrate concentrated till dryness. The resulting solid was dissolved in saturated sodium bicarbonate solution and the aqueous layer extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to afford solid methyl 3-amino-2-methyl-5-(trifluoromethyl)benzoate in quantitative yield.

Workup

  1. customthe resulting reaction mixture
  2. filtrationOn completion, the reaction mixture was filtered
  3. concentrationthe filtrate concentrated till dryness
  4. dissolutionThe resulting solid was dissolved in saturated sodium bicarbonate solution
  5. extractionthe aqueous layer extracted with ethyl acetate
  6. dry with materialThe combined organic layers were dried over sodium sulfate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-c3e1b3dd693b41298c4cfac8ee131de7
Source dataset
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09206157B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes