Reaktionsgleichung
[CH:1]1[C:23]2=[C:24]3[C:4]4[C:5]([CH:17]=[CH:18][C:19]3=[C:20](S([O-])(=O)=O)[CH:21]=[C:22]2[OH:25])=[C:6](S([O-])(=O)=O)[CH:7]=[C:8](S([O-])(=O)=O)[C:3]=4[CH:2]=1.[Na+:30].[Na+].[Na+].[S:33](=O)(=[O:36])([OH:35])[OH:34]>>[OH:25][C:22]1[CH:21]=[CH:20][C:19]2[C:24]3=[C:4]4[C:5]([CH:6]=[CH:7][CH:8]=[C:3]4[C:2]([S:33]([O-:36])(=[O:35])=[O:34])=[CH:1][C:23]=13)=[CH:17][CH:18]=2.[Na+:30]Komponenten
3
Versuchsvorschrift
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.
Quellen und Nachweise
- ORD-Eintrag
- ord-d2ac55930bfd49cd8c31bca9633c57ff
- Quelldatensatz
- uspto-grants-2010_11
- Patentnummer
- US07824918B2
Verknüpfte Notizen
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