Реакция #1256732

ord-d2ac55930bfd49cd8c31bca9633c57ff

Уравнение реакции

O=S(=O)([O-])c1cc(O)c2ccc3c(S(=O)(=O)[O-])cc(S(=O)(=O)[O-])c4ccc1c2c34.[Na+].[Na+].[Na+]
HPTS
O=S(=O)(O)O
sulfuric acid
→
O=S(=O)([O-])c1cc2c(O)ccc3ccc4cccc1c4c32.[Na+]
sodium 3-hydroxypyrene-5-sulfonate
Выход 10.0%

Реактанты

—
compound 3
O=S(=O)([O-])c1cc(O)c2ccc3c(S(=O)(=O)[O-])cc(S(=O)(=O)[O-])c4ccc1c2c34.[Na+].[Na+].[Na+]
HPTS
O=S(=O)(O)O
sulfuric acid

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Scheme 1 shows steps used to synthesize compound 3. Reaction of HPTS with 30% sulfuric acid at 150° C. for 20 min gave sodium 3-hydroxypyrene-5-sulfonate 1 in 10% yield. Acetylation of 1 followed by chlorination of 2 gave intermediate 3, which is analogous to our HPTS-Cl but with only one sulfonyl chloride.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07824918B2uspto-grants-2010_11