HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-((Tetrahydro-2H-pyran-2-YL)oxy)cyclopropane-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ethyl 2-(oxan-2-yloxy)cyclopropane-1-carboxylate | HCID 22325102 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-((Tetrahydro-2H-pyran-2-YL)oxy)cyclopropane-1-carboxamide | HCID 22325163 | — |
Reaction Steps
In an autoclave, a solution of 0.25 mol of the compound obtained in Step 2, 2 g of sodium cyanide, 300 ml of a 2N solution of ammonia in methanol and 80 ml of liquid ammonia is heated at 65° C. for 5 days and is then concentrated to dryness. The residue is taken up in a mixture of dichloromethane/saturated potassium carbonate solution, filtered over Celite and then treated in conventional manner. After evaporating under reduced pressure, the residue is triturated in petroleum ether, filtered, rinsed and dried, allowing the expected product to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06943184B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-37dccb7e6302428a9e079c22d310f0b7 |
| Source note | uspto-grants-2005_09 |