HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroethane → HCID 12875760, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroethane | HCID 6337 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one | HCID 88638 | — |
| Reactant | HCID 131712197 | HCID 131712197 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 12875760 | HCID 12875760 | 107.7% |
Reaction Steps
A suspension of 6.87 g of 3,4-dihydroxyphenyl chloromethylketone (trade product) and 8 g of 4-(2-oxobenzimidazolin-1-yl)piperidine (trade product), M.P. 183°-185° C., in 640 ml of methylethyl ketone, in the presence of 1.95 g of dried sodium carbonate and 0.1 g of sodium iodide, was refluxed for 12 hours. After the completion of the reaction, the precipitate was filtered off and washed with water. After drying, there were obtained 14 g of raw base which is transformed in hydrochloride in methanol by addition of hydrochloric ether. There were obtained 8 g of 1-(3,4-dihydroxy phenacyl)-4-(2-oxobenzimidazolin-1-yl)piperidine hydrochloride, white crystals melting at 310°-313° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04264613 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-e15e5995276f4fe89dd59790964cf37c |
| Source note | uspto-grants-1981_04 |