Reacción #2045057

ord-abe69e4c688f404f9e731a921127110a

Ecuación de reacción

O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[Na+]
sodium iodide
O=P([O-])([O-])O.[Na+].[Na+]
disodium phosphate
COC(=O)CCl
methylchloroacetate
COC(=O)CCl
Methylchloroacetate
O=C(O)c1ccccc1O
salicylic acid
CCN(CC)CC
triethylamine
COC(=O)COC(=O)c1ccccc1OCC(=O)OC
93
COC(=O)COC(=O)c1ccccc1OCC(=O)OC
2-Methoxycarbonylmethoxy-benzoic acid methoxycarbonylmethyl ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturato reflux for 10 hrs
  3. 3
    FiltraciónSolids were filtered off
  4. 4
    Temperaturarefluxed for 16 hrs
  5. 5
    workup.DISTILLATIONAcetone was distilled off
  6. 6
    workup.ADDITIONwater (125 ml) added
  7. 7
    ExtracciónCrude 93 was extracted into chloroform
  8. 8
    Lavadowashed with 5% sodium bicarbonate solution (2×50 ml), with water (2×50 ml)
  9. 9
    Secadodried over sodium sulphate
  10. 10
    workup.DISTILLATIONdistilled
  11. 11
    OtroCrude 93 was purified by column chromatography on silica gel

Procedimiento

Methylchloroacetate (9.4 g, 86.66 mmol) was added dropwise to a mixture of salicylic acid (10 g, 72.46 mmol) and triethylamine (8.8 g, 86.96 mmol) in acetone (50 ml) and heated to reflux for 10 hrs. Solids were filtered off and potassium carbonate (25 g, 180.89 mmol) was added to the acetone layer together with sodium iodide (2 gm, 13.34 mmol), disodium phosphate (2 g, 14.16 mmol) and methylchloroacetate (9.4 g, 86.66 mmol) and refluxed for 16 hrs. Acetone was distilled off and water (125 ml) added. Crude 93 was extracted into chloroform, washed with 5% sodium bicarbonate solution (2×50 ml), with water (2×50 ml), dried over sodium sulphate and distilled. Crude 93 was purified by column chromatography on silica gel using benzene to get pure 93 (12 g, 58.7%) as a syrup.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08409559B2uspto-grants-2013_04