Acetic Acid → (Nitromethyl)benzene

HRID 1460864Notes

Reaction equation

HRID 1460864 reaction equation
[CH:1](=[N:8][OH:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(O)(=[O:12])C.C(OO)(=O)C.O.O.O.C([O-])(=O)C.[Na+]>O>[N+:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)([O-:12])=[O:9]

Participants

6

Conditions

Temperature
80 °C

Procedure

184.1 g. (1.51 mole) of benzaldehyde oxime and 185 ml. of glacial acetic acid are placed in a 3 liter 3 neck flask. The mixture is stirred and heated to 80° C. A solution of 344.1 g. (1.65 mole) of 36.6% peracetic acid and 19 g. of sodium acetate trihydrate is added at a rate such that the temperature is maintained between about 80° and about 90° C. Stirring is continued at about 85° C. for about 3 1/2 hours until there is no oxime. The reaction mixture is chilled to 25° C. and one liter of water is added and the mixture stirred well and the oil which forms, is separated. The aqueous layer is extracted twice with 200 ml. of methylene chloride. The aqueous extract is combined with the oil layer and washed twice with 600 ml. of water and once with 600 ml. of 5% sodium bicarbonate solution, washed again with 400 ml. of water, and dried over sodium sulfate and concentrated to a light orange oil. The yield is 173.5 g. (84%) of 97% pure material by GC.

Workup

  1. temperatureis maintained between about 80° and about 90° C
  2. stirringStirring
  3. customis continued at about 85° C. for about 3 1/2 hours until there
  4. temperatureThe reaction mixture is chilled to 25° C.
  5. stirringthe mixture stirred well
  6. customis separated
  7. extractionThe aqueous layer is extracted twice with 200 ml
  8. extractionThe aqueous extract
  9. washwashed twice with 600 ml
  10. washof 5% sodium bicarbonate solution, washed again with 400 ml
  11. dry with materialof water, and dried over sodium sulfate
  12. concentrationconcentrated to a light orange oil

Sources & evidence

ORD record
ord-8b1572ed5bcc4c4db702c26170e72ed4
Source dataset
uspto-grants-1991_12
Patent number
US05072056

Reaction notes

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