Ammonium Chloride → Methyl 3-Amino-5-bromo-2-methylbenzoate

HRID 1501682Notes

Reaction equation

HRID 1501682 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([N+:13]([O-])=O)[C:5]([CH3:12])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].[NH4+].[Cl-]>C(O)C.[Fe]>[NH2:13][C:4]1[C:5]([CH3:12])=[C:6]([CH:11]=[C:2]([Br:1])[CH:3]=1)[C:7]([O:9][CH3:10])=[O:8]

Participants

5

Conditions

Temperature
90 °C

Procedure

A mixture of methyl 5-bromo-2-methyl-3-nitrobenzoate (17 g, 62.0 mmol) in ethanol (85 mL) had NH4Cl solution (17 g in 85 mL water, 317.8 mmol) followed by Fe powder (27.8 g, 498.1 mmol) added. The resulting reaction mixture was stirred at 90° C. for 1 h. On completion, the reaction mixture was filtered and the filtrate was concentrated till dry. The resulting solid was dissolved in sat. sodium bicarbonate solution and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to afford solid methyl 3-amino-5-bromo-2-methylbenzoate (15 g, 99.1%).

Workup

  1. additionadded
  2. customThe resulting reaction mixture
  3. filtrationOn completion, the reaction mixture was filtered
  4. concentrationthe filtrate was concentrated
  5. customtill dry
  6. dissolutionThe resulting solid was dissolved in sat. sodium bicarbonate solution
  7. extractionextracted with ethyl acetate
  8. dry with materialThe combined organic layers were dried over sodium sulfate
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-087df476307f45d8abe695737ff735a1
Source dataset
uspto-grants-2015_12
Patent number
US09206157B2

Reaction notes

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