Reacción #2267060

ord-d385c4fe70c543bfbb5e2b0d48e714e2

Ecuación de reacción

O=C(O)c1ccc2cc(O)ccc2c1
6-hydroxy-2-naphthoic acid
[Na+].[O-]Cl
NaOCl
O=S([O-])S(=O)(=O)[O-].[Na+].[Na+]
sodium metabisulfite
Cl
HCl
O=C(O)c1ccc(O)cc1
4-hydroxybenzoic acid
[I-].[Na+]
NaI
[Na+].[OH-]
NaOH
O=C(O)c1ccc2c(I)c(O)ccc2c1
5-iodo-6-hydroxy-2-naphthoic acid

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added dropwise over 75 min
  2. 2
    Extracciónextracted with 40 ml of ether
  3. 3
    LavadoThe organic layer was washed with brine
  4. 4
    Secadodried over MgSO4
  5. 5
    ConcentraciónThe solution was concentrated to an off-white solid, that
  6. 6
    Otrowas recrystallized from toluene/CH3OH

Procedimiento

Mono-iodination of 6-hydroxy-2-naphthoic acid and 4-hydroxybenzoic acid was carried out following the procedure of Edgar and Falling (J. Org. Chem. 55, 5287, 1990). Thus, 0.75 gm of (4.34 mmol) was dissolved in 19 ml of MeOH and 1.04 gm of NaI (and 0.27 gm of NaOH was added. The solution was cooled to O▪C and aqueous NaOCl (4% solution, 12.9 ml) was added dropwise over 75 min. The resulting mixture was stirred for 1 hr at 0° C. and then treated with 7 ml of 10% aqueous sodium metabisulfite. The mixture was adjusted to pH 7 using 5% HCl and extracted with 40 ml of ether. The organic layer was washed with brine and dried over MgSO4. The solution was concentrated to an off-white solid, that was recrystallized from toluene/CH3OH to provide 0.42 gm of 5-iodo-6-hydroxy-2-naphthoic acid. Reaction of 6′-Tostylatractviloside with 1.2-ethylenediamine

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06887670B2uspto-grants-2005_05