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

HRID 1854129Notes

Reaction equation

HRID 1854129 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-c3df75779ead4b168c34c2895d6110dc
Source dataset
uspto-grants-2015_02
Patent number
US08962620B2

Reaction notes

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