Reaction #543541

ord-db9272fcc54841b88676ea04e0f46721

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe reaction mixture was maintained below 5° C. during the addition
  2. 2
    workup.STIRRINGstirred at 5° C. for an additional 2 h
  3. 3
    OtherThe solid formed
  4. 4
    Filtrationwas filtered
  5. 5
    Washwashed with cold ether:ethanol (3:1, 150 mL)
  6. 6
    Otherdried
  7. 7
    OtherIt was crystallized from acetonitrile

Procedure

To a cooled (0-5° C.) solution of 4-methyl-1-(phthalimido)-3-pentene (5.0 g, 0.022 mol) and isoamyl nitrite (13.0 g, 15 mL, 0.11 mol) was added concentrated hydrochloric acid (4.0 mL, 0.04 mol) with stirring. The reaction mixture was maintained below 5° C. during the addition and stirred at 5° C. for an additional 2 h. The solid formed was filtered and washed with cold ether:ethanol (3:1, 150 mL) and dried. Yield: 4.72 g (72.8%). It was crystallized from acetonitrile. mp 140-141° C. MS: (M+H)+=296.0.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07186397B2uspto-grants-2007_03