Réaction #1328407

ord-60c5e1bbaeb54e9ab91ffdc73e33254f

Équation de réaction

CCOC(C)=O
EtOAc
CC(=O)c1ccc2c(c1)OCO2
3,4-methylenedioxy-acetophenone
O=[N+]([O-])O
HNO3
CC(=O)c1cc2c(cc1[N+](=O)[O-])OCO2
4,5-methylenedioxy-2-nitroacetophenone

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction
  2. 2
    Températurewithout external cooling from an ice bath
  3. 3
    AutreAt temperatures below 0° C., however, the reaction
  4. 4
    AutreA temperature of 3–5° C.
  5. 5
    workup.WAITThe mixture was left
  6. 6
    workup.STIRRINGstirring for another 60 minutes at 3–5° C.
  7. 7
    Autreto approach ambient temperature
  8. 8
    Autrewithin 1–2 hr
  9. 9
    Filtrationthe resulting yellow solid was filtered off
  10. 10
    Lavagewashed with water
  11. 11
    Autresuction-dried
  12. 12
    AutreYield 53 g (84%), used without further purification

Mode opératoire

A solution of 50 g (0.305 mole) 3,4-methylenedioxy-acetophenone (Aldrich) in 200 mL glacial acetic acid was added dropwise over 30 minutes to 700 mL of cold (2–4° C.) 70% HNO3 with stirring (NOTE: the reaction will overheat without external cooling from an ice bath, which can be dangerous and lead to side products). At temperatures below 0° C., however, the reaction can be sluggish. A temperature of 3–5° C. seems to be optimal). The mixture was left stirring for another 60 minutes at 3–5° C., and then allowed to approach ambient temperature. Analysis by TLC (25% EtOAc in hexane) indicated complete conversion of the starting material within 1–2 hr. When the reaction was complete, the mixture was poured into ˜3 liters of crushed ice, and the resulting yellow solid was filtered off, washed with water and then suction-dried. Yield 53 g (84%), used without further purification.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07115364B1uspto-grants-2006_10