HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 2-Benzyl-5-cyanomethyl-2,5-diazabicyclo[2.2.1]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Benzyl-2,5-diazabicyclo[2.2.1]heptane | HCID 562932 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Benzyl-5-cyanomethyl-2,5-diazabicyclo[2.2.1]heptane | HCID 21963645 | — |
Reaction Steps
Finely ground potassium carbonate, as well as 1.3 mL of freshly distilled chloroacetonitrile were added to a solution of 3 g of 2-benzyl-2,5-diazabicyclo[2.2.1]heptane in 40 mL of anhydrous toluene and refluxed for 10 hours with vigorous stirring. The solution was cooled, filtered and evaporated. Bulb tube distillation (boiling point: 110°-120° C. at 0.01 mbar) resulted in 3.57 g of 140 as a colorless oil (97% of the theoretical yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06638925B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-b74a3b1c9a3f4525a31d3bb55d105ccf |
| Source note | uspto-grants-2003_10 |