Ethyl Acetate → 4-Bromo-2-methoxy-6-methylaniline

HRID 2194796Notes

Reaction equation

HRID 2194796 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:4]=1[NH2:10].[Br:11]Br.C(OCC)(=O)C>CO.C(O)(=O)C>[Br:11][C:7]1[CH:6]=[C:5]([CH3:9])[C:4]([NH2:10])=[C:3]([O:2][CH3:1])[CH:8]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

In a 100 mL round bottom flask, 2-methoxy-6-methyl-phenylamine (4.54 g, 33.16 mmol) was dissolved in 15 mL MeOH and 5 mL acetic acid. The flask was cooled to 0° C. Bromine (1.7 mL, 33.16 mmol) in 5 mL acetic acid was added to the reaction dropwise (over 30 minutes). The reaction mixture was stirred at 0° C. for 2 hours, then was warmed up to room temperature for 1 hour. The reaction mixture was concentrated down. 1N NaOH was added to neutralize the reaction at 0° C. Ethyl acetate was added to extract the reaction mixture. The organic layer was concentrated after drying over anhydrous sodium sulfate to give a dark brown solid (5.8 g, 81%). LC-MS shows 218.0 (M+1). 1H NMR (300 MHz, CDCl3): δ 6.88 (s, 1H), 6.81 (s, 1H), 3.84 (s, 3H), 2.11 (s, 3H).

Workup

  1. temperaturewas warmed up to room temperature for 1 hour
  2. concentrationThe reaction mixture was concentrated down
  3. addition1N NaOH was added
  4. customthe reaction at 0° C
  5. extractionto extract the reaction mixture
  6. concentrationThe organic layer was concentrated
  7. dry with materialafter drying over anhydrous sodium sulfate

Sources & evidence

ORD record
ord-a8f806df7efb4b13a3d553d7a8a5f103
Source dataset
uspto-grants-2012_12
Patent number
US08334295B2

Reaction notes

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