HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 2-(4-piperidinylmethyl)-1-(2-thienylmethyl)-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 10845171 | HCID 10845171 | — |
| Reactant | HCID 14012872 | HCID 14012872 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-piperidinylmethyl)-1-(2-thienylmethyl)-1H-benzimidazole | HCID 14012874 | 49% |
Reaction Steps
A mixture of 68 parts of ethyl 4-[[1-(2-thienylmethyl)-1H-benzimidazol-2-yl]methyl]-1-piperidinecarboxylate monohydrochloride, 95 parts of potassium hydroxide, 800 parts of 2-propanol and 10 parts of water was stirred and refluxed for 6 hours. The reaction mixture was evaporated and water was added to the residue. The product was extracted with methylbenzene. The extract was dried, filtered and evaporated. The residue was crystallized from 1,1'-oxybisethane. The product was filtered off and dried, yielding 27 parts (49%) of 2-(4-piperidinylmethyl)-1-(2-thienylmethyl)-1H-benzimidazole; mp. 117.4° C. (64).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04839374 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-61aa3fec301d44b5b09ab7a3e4702d6e |
| Source note | uspto-grants-1989_06 |