Ammonia → 4-Aminomethyl-3-nitrobenzoic acid

HRID 2264091Notes

Reaction equation

HRID 2264091 reaction equation
Br[CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][C:4]=1[N+:12]([O-:14])=[O:13].[NH3:15]>CCO>[NH2:15][CH2:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][C:4]=1[N+:12]([O-:14])=[O:13]

Participants

4

Procedure

4-(Bromomethyl)-3-nitrobenzoic acid (3.2 g; 12.3 mmol) was dissolved in 8% NH3 in EtOH (300 mL) and the resulting solution was stirred at room temperature. After 22 h the solution was evaporated and the residue suspended in H2O (70 mL). The suspension was stirred for 15 min and filtered. The collected solid was suspended in H2O (40 mL) and dissolved by the addition of few drops of 25% aq. NH4OH (pH 12), then the pH of the solution was adjusted to 6 by addition of 6 N HCl. The precipitated solid was filtered, and washed sequentially with MeOH (3×5 mL), and Et2O (10 mL) and was vacuum dried (1.3 kPa; P2O5) to give 4-(aminomethyl)-3-nitrobenzoic acid as a pale brown solid (1.65 g; 8.4 mmol). Yield 68%.

Workup

  1. customAfter 22 h the solution was evaporated
  2. stirringThe suspension was stirred for 15 min
  3. filtrationfiltered
  4. dissolutiondissolved by the addition of few drops of 25% aq. NH4OH (pH 12)
  5. additionthe pH of the solution was adjusted to 6 by addition of 6 N HCl
  6. filtrationThe precipitated solid was filtered
  7. washwashed sequentially with MeOH (3×5 mL), and Et2O (10 mL)
  8. dry with materialdried (1.3 kPa; P2O5)

Sources & evidence

ORD record
ord-8dc998f717254c32bc9831b9ee47b0d3
Source dataset
uspto-grants-2010_12
Patent number
US07850947B2

Reaction notes

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