HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzenesulfonyl chloride → 4-Nitrobenzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Azide | HCID 33558 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Reactant | Nosylate | HCID 4215492 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Product | 4-Nitrobenzenesulfonyl azide | HCID 542778 | — |
Reaction Steps
Secondary alcohol 7 was converted to azide 8 through the formation of a secondary nosylate using 4-nitrobenzenesulfonyl chloride and 4-pyrrolidinopyridine in chloroform followed by azide displacement with sodium azide in N,N-dimethylformamide at 50° C. The p-methoxy trityl protecting group was selectively removed using 1% p-toluenesulfonic acid in methylene chloride. Nosylation of the primary alcohol with 4-nitrobenzenesulfonyl chloride and pyridine in chloroform provided azido-nosylate 9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150416 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-56c77319f5ac48d79f7584bb9355f664 |
| Source note | uspto-grants-2000_11 |