HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Benzyloxypyridine → N-amino-3-benzyloxypyridinium mesitylenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Benzyloxypyridine | HCID 10012635 | — |
| Reactant | O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine | HCID 11830845 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-amino-3-benzyloxypyridinium mesitylenesulfonate | HCID 15257892 | — |
Reaction Steps
A solution of O-mesitylenesulfonylhydroxylamine (13.7 g, 44.6 mmole, purity of 70%) in methylene chloride (150 ml) was added dropwise to a solution of 3-benzyloxypyridine (8.25 g, 44.6 mmole) in methylene chloride (150 ml) under ice-cooling, with stirring. The reaction solution was returned to room temperature, stirred for 1 hours and concentrated to one-quarter of the original volume at 20° to 30° C., and ether was added to the concentrate, thereby white crystals were precipitated. This product was used in the next reaction, without being purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05202334 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-a37ccfad46eb4f3ca7b8a6def85f67d4 |
| Source note | uspto-grants-1993_04 |