HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 178506598, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 178504030 | HCID 178504030 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178506598 | HCID 178506598 | — |
Reaction Steps
To a suspension of 9.61 g (0.025 mole) of methyl-N-(diphenylmethyl)-carbamimidothioate hydroiodide in 20 ml of t-BuOH is added 4.26 g (0.05 mole) of piperidine. The mixture is heated under reflux over night. The resulting crystals after cooling in ice, are filtered; mp 200°-213° C. One recrystallization from methanol-t-BuOH yields the pure product, N-(diphenylmethyl)-1-piperidinecarboximidamide monohydroiodide as a white crystalline solid; mp 207°-210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04161541 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-c0aae1c572ea496db40d3e4c51b465fb |
| Source note | uspto-grants-1979_07 |