HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 178425552, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 178504032 | HCID 178504032 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 178425552 | HCID 178425552 | — |
Reaction Steps
A mixture of 13.3 g (0.0334 mole) of methyl N-(4-methylbenzhydryl)carbamimidothioate hydroiodide and 5.0 g (0.07 mole) of pyrrolidine in 40 mls of t-BuOH is heated under reflux for 24 hrs. The crude product crystallizes out of the reaction mixture while refluxing. The mixture is allowed to cool over night at room temperature and filtered to yield crude product; mp 227°-30° C. Recrystallization from MeOH/t-BuOH yields the pure N-(4-methylbenzhydryl)-1-pyrrolidinecarboximidamide hydroiodide; mp 229°-230° C, as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101659 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-f8fb022e66914754bfdaed45c78befa2 |
| Source note | uspto-grants-1978_07 |