Reacción #2267060
ord-d385c4fe70c543bfbb5e2b0d48e714e2
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas added dropwise over 75 min
- 2Extracciónextracted with 40 ml of ether
- 3LavadoThe organic layer was washed with brine
- 4Secadodried over MgSO4
- 5ConcentraciónThe solution was concentrated to an off-white solid, that
- 6Otrowas 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