Hydrochloric Acid → 2-Methoxy-4-methylbenzenemethanamine

HRID 1518591Notes

Reaction equation

HRID 1518591 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([CH3:12])[CH:9]=[CH:8][C:4]=1[C:5]([NH2:7])=O.B.O1CCCC1.Cl.O>C1COCC1>[CH3:1][O:2][C:3]1[CH:11]=[C:10]([CH3:12])[CH:9]=[CH:8][C:4]=1[CH2:5][NH2:7]

Participants

6

Conditions

Temperature
60 °C

Procedure

To a solution of 2-methoxy-4-methylbenzamide (14.55 g, 88.08 mmol) in dry THF (50 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 220 mL, 2.5 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq.HCl (6 N, 37 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated to give 8.5 g of (2-methoxy-4-methylphenyl)methanamine. (64% yield)

Workup

  1. temperatureThe reaction was cooled to room temperature
  2. temperaturethe reaction mixture was then heated at 70° C. for 2 hrs
  3. temperatureAfter cooling
  4. washthe resulting solution was washed with ether
  5. customwas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
  6. extractionthen extracted with ethyl acetate
  7. washThe organic layer was washed with brine
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customevaporated

Sources & evidence

ORD record
ord-9332be9bf76d476dacd2441d061bee3e
Source dataset
uspto-grants-2015_07
Patent number
US09072313B2

Reaction notes

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