HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine | HCID 11830845 | — |
| Reactant | 2-(1-Butynyl)pyridine | HCID 21299391 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate | HCID 21984654 | 39.1% |
Reaction Steps
After dissolving 2-(1-butynyl)pyridine (12.8 g) in dichloromethane (60 mL), a solution of O-mesitylenesulfonylhydroxyamine (Reference document: Synthesis, 1997, 1) (20 g) in dichloromethane (132 mL) was added dropwise while cooling on ice, and the mixture was stirred for 30 minutes. Diethyl ether (2 L) was added to the reaction mixture to precipitate crystals, which were collected by filtration and dried under reduced pressure to obtain N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate (12.6 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091215B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a32947a36a4c48d3857c5a4f444f36ff |
| Source note | uspto-grants-2006_08 |