HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 6-(1-Pyrenebutyryl)-3,6,10,16-tetraazabicyclo[10.3.1]-hexadeca-1(16),12,14-triene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-(1-Pyrenebutyryl)-3,10-bis(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1(16),12,14-triene | HCID 10724280 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(1-Pyrenebutyryl)-3,6,10,16-tetraazabicyclo[10.3.1]-hexadeca-1(16),12,14-triene | HCID 10553094 | 87.8% |
Reaction Steps
A mixture of 6-(1-Pyrenebutyryl)-3,10-bis(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]-hexadeca-1(16),12,14-triene (2.26 g, 2.6 mmol), thiphenol (0.87 g, 7.8 mmol) and K2CO3 (3.22 g, 23.4 mmol) in 20 mL of DMF was stirred at rt overnight. The solvent was evaporated and the residue was dissolved in CHCl3—H2O. The organic phase was separated and the aqueous phase was extracted with CHCl3. The combined organic phase was dried (Na2SO4) and concentrated. The residue was purified by flash chromatography on a silica gel column using CH2Cl2 and then 3:1 CH2Cl2—MeOH as eluents to give 1.12 g (65%) of the title compound as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191273B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-0bb5170e162e468dbffe3a5ccdbf1189 |
| Source note | uspto-grants-2001_02 |