HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354990Generated: October 30, 2026
Hydrochloric Acid → HCID 13105579, compound
https://huagongshe.com/reaction/354990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 20506317 | HCID 20506317 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13105579 | HCID 13105579 | — |
Reaction Steps
To a stirred solution of 9.6 parts of 3-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-5-methyl-1-(1-methylethenyl)-2H-benzimidazol-2-one in 80 parts of ethanol are added 24 parts of a concentrated hydrochloric acid solution and 50 parts of water (exothermic reaction: temperature rises to 50° C.). Stirring is continued for 30 minutes at room temperature. The reaction mixture is evaporated and the residue is triturated in 2-propanone. The hydrochloride salt is filtered off and the free base is liberated in the conventional manner with ammonium hydroxide. Methylbenzene is added and the precipitated free base is filtered off. It is crystallized from a mixture of 2-propanol and a small amount of N,N-dimethylformamide, yielding 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-6-methyl-2H-benzimidazol-2-one; mp. 195.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377578 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-54e7a28eeeb24862b30963b69c50d718 |
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| Source note | uspto-grants-1983_03 |
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