Reacción #2787

ord-b61bb71ca3fc444f88d24d728812b5de

Ecuación de reacción

O
water
c1c[nH]cn1
imidazole
C=C(P(=O)(OC)OC)S(=O)(=O)OC
methyl 1-dimethoxyphosphinylethenesulfonate
C[Si](C)(C)Br
bromotrimethylsilane
O=P(O)(O)C(Cn1ccnc1)S(=O)(=O)O
2-(1-imidazolyl)-1-phosphonoethanesulfonic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe mixture is stirred for about 30 minutes
  2. 2
    Otrothe layers are separated
  3. 3
    ExtracciónThe water layer is extracted several times with CHCl3 (extracts are discarded)
  4. 4
    Otrois evaporated to dryness under vacuum
  5. 5
    OtroThe residue is triturated with acetone
  6. 6
    Otroto give a solid, which
  7. 7
    Filtraciónis collected by filtration
  8. 8
    Otrorecrystallized from water/acetone

Procedimiento

A mixture of 0.68 g (0.01 mole) of imidazole and 2.30 g (0.01 mole) of methyl 1-dimethoxyphosphinylethenesulfonate (U.S. Pat. No. 5,011,938 issued to Barnett et al. on Apr. 30, 1991) in 20 ml of chloroform is stirred at 20°-50° for one day. The reaction is cooled to room temperature, and 10.7 g (0.07 mole) of bromotrimethylsilane is added. The mixture is stirred at 20°-30° for 2-3 days, and to it is then added 20 ml water. The mixture is stirred for about 30 minutes, and the layers are separated. The water layer is extracted several times with CHCl3 (extracts are discarded) and is evaporated to dryness under vacuum. The residue is triturated with acetone to give a solid, which is collected by filtration and recrystallized from water/acetone to afford 2-(1-imidazolyl)-1-phosphonoethanesulfonic acid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05731299uspto-grants-1998_03