HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → 4-(N,S-Dimethylsulfonimidoyl)benzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(4-(N,S-Dimethylsulfonimidoyl)benzyl)isoindoline-1,3-dione | HCID 86711642 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(N,S-Dimethylsulfonimidoyl)benzylamine | HCID 86711643 | — |
Reaction Steps
A mixture of 2-(4-(N,S-dimethylsulfonimidoyl)benzyl)isoindoline-1,3-dione (189 mg, 0.58 mmol) and 1,2-diaminoethane (132 μL, 3.44 mmol) in a 2:1:1 mixture of acetonitrile, tetrahydrofuran and ethanol (2 mL) is heated at reflux for 1 h. All volatiles are removed under reduced pressure, and the residue is treated with dichloromethane. The mixture is filtered, and the filtrate is concentrated under reduced pressure. Yield: 114 mg (85% of theory); ESI mass spectrum: [M+H]+=199; r.t. HPLC: 0.22 min (X011_S03).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346794B1 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-e79c3980c4ee481c8d121f645d85ca49 |
| Source note | uspto-grants-2016_05 |