Nitric Acid → 6-Methyl-1,3-dioxaindan-5-amine

HRID 1841404Notes

Reaction equation

HRID 1841404 reaction equation
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([CH3:10])=[CH:4][C:3]=2[O:2]1.[N+:11]([O-])(O)=O.O>C(O)(=O)C>[CH2:1]1[O:2][C:3]2[CH:4]=[C:5]([CH3:10])[C:6]([NH2:11])=[CH:7][C:8]=2[O:9]1

Participants

5

Procedure

To a solution of (3,4-methylenedioxy)toluene (5 ml) in acetic acid (20 ml) cooled with a cold water bath was added, dropwise, nitric acid (70%, 5 ml). The mixture was stirred for 45 min. To work up, water (100 ml) was added and the resulting yellow precipitate was filtered and washed with water until the aqueous filtrate was colorless. The yellow solid was dissolved in EtOAc (250 ml) and dried (MgSO4), and the solid was filtered off. The filtrate was subjected to catalytic hydrogenation (1 0% Pd/C, 1 atm) for 1 2 hours. The reaction mixture was then filtered off the catalyst and the filtrate was concentrated on a rotavap to give (3,4-methylenedioxy)-6-methylaniline as a brownish grey solid (5.49 g, 87% yield).

Workup

  1. additionwas added
  2. filtrationthe resulting yellow precipitate was filtered
  3. washwashed with water until the aqueous filtrate
  4. dissolutionThe yellow solid was dissolved in EtOAc (250 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationthe solid was filtered off
  7. customwas subjected to catalytic hydrogenation (1 0% Pd/C, 1 atm) for 1 2 hours
  8. filtrationThe reaction mixture was then filtered off the catalyst
  9. concentrationthe filtrate was concentrated on a rotavap

Sources & evidence

ORD record
ord-fa486bddcac14048b964826e6924413b
Source dataset
uspto-grants-2004_01
Patent number
US06683103B2

Reaction notes

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