HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 178506599, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 178504034 | HCID 178504034 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178506599 | HCID 178506599 | — |
Reaction Steps
A mixture of 7.0 g (0.017 mole) of methyl N-(4-chlorobenzhydryl)carbamimidothioate hydroiodide and 2.85 g (0.04 mole) of pyrrolidine in 20 mls of t-BuOH is heated at reflux overnight. The t-BuOH is removed in vacuo and the crude guanidine hydroiodide is crystallized from methanol-ether. The crude product is recrystallized from methanol-t-butanol to yield pure N-(4-chlorobenzhydryl)-1-pyrrolidinecarboximidamide hydroiodide; mp 218°-220° (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101659 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-225a5d08e14f419c8dc486594e2658c3 |
| Source note | uspto-grants-1978_07 |