HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,3-Diiodopropane | HCID 12314 | — |
| Reactant | 1,4,7-Triazacyclononane | HCID 188318 | — |
| Reactant | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| Product | HCID 17939386 | HCID 17939386 | — |
Reaction Steps
N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-Bis[N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluenesulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06387891B2 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-b718a5cbb0b444359a2bff50bdcc59e6 |
| Source note | uspto-grants-2002_05 |