Réaction #487499

ord-ec54f0937fb144ff9a32b4631bb00133

Équation de réaction

Nc1ccccc1
aniline
c1ccc(P(CCP(c2ccccc2)c2ccccc2)c2ccccc2)cc1
1,2-bis(diphenylphosphino)ethane
[N-]=[N+]=Nc1ccccc1
phenylazide
C1CCOC1
THF
O=C(Nc1ccccc1)Nc1ccccc1
Diphenylurea

Conditions de réaction

Température
120°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas pre-charged with [11C]CO
  2. 2
    Autrewas flushed with N2 (the [11C]CO-
  3. 3
    AutreA small amount of crude product was collected

Mode opératoire

In a capped vial (1 mL) containing a solution of phenylazide (6.6 mg, 55 μmol) in dry THF (300 μL), was added [RhCl(cod)]2 (0.27 mg, 0.55 μmol), and 1,2-bis(diphenylphosphino)ethane (0.44 mg, 1.1 μmol) and was shaken until the solution was homogeneous. After addition of aniline (10 μL, 110 μmol), the resulting mixture was transferred to the micro-autoclave, which was pre-charged with [11C]CO. The autoclave (250 μL) was heated at 120° C. for 5 min under 35 MPa and the crude product was transferred to a reduced pressure vial. The radioactivity was measured before and after the vial was flushed with N2 (the [11C]CO-trapping efficiency of 82% was determined based on these values). A small amount of crude product was collected and analyzed by the reversed phase HPLC. Yield of product: 82%. The product was identified by HPLC with an added authentic reference compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08741261B2uspto-grants-2014_06