Réaction #725939

ord-ca0b7bacaa164ede86aeaeddcb262315

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureheated
  2. 2
    Températureto reflux for 10 hrs
  3. 3
    FiltrationSolids were filtered off
  4. 4
    Températurerefluxed for 16 hrs
  5. 5
    workup.DISTILLATIONAcetone was distilled off
  6. 6
    workup.ADDITIONwater (125 ml) added
  7. 7
    ExtractionCrude 93 was extracted into chloroform
  8. 8
    Lavagewashed with 5% sodium bicarbonate solution (2×50 ml), with water (2×50 ml)
  9. 9
    Séchagedried over sodium sulphate
  10. 10
    workup.DISTILLATIONdistilled
  11. 11
    AutreCrude 93 was purified by column chromatography on silica gel

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07691364B2uspto-grants-2010_04