HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → 1-Benzyl-1,4,7,10-tetraazacyclododecane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 4-Benzyl-1,4,7,10-tetraazacyclododecane-2,6-dione | HCID 15702829 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Benzyl-1,4,7,10-tetraazacyclododecane | HCID 10084082 | — |
Reaction Steps
To a suspension of 890 mg (3.07 mmol) of 1-benzyl-3,11-dioxo-1,4,7,10-tetraazacyclododecane in tetrahydrofuran under nitrogen was added 2.64 ml of 8M borane-methyl sulfide complex (21.1 mol, 7 equivalents). The mixture was heated to reflux allowing the methyl sulfide to distill out of the reaction flask. After 2 hours, the reaction was quenched by the addition of 12 ml 1.8M hydrochloric acid in methanol and refluxed for an additional 3 hours. Volatiles were removed by evaporation, and the solid resuspended in methanol and reevaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05674470 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-a615d76bb934411d9115296ff4afe4a6 |
| Source note | uspto-grants-1997_10 |