HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448095Generated: October 31, 2026
Ethyl orthoformate → HCID 20298824, compound
https://huagongshe.com/reaction/1448095
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 53790858 | HCID 53790858 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 20298824 | HCID 20298824 | — |
Reaction Steps
A mixture of 5 parts of 4-[4-(diphenylmethyl)-1-piperazinylmethyl]-N1 -propyl-1,2-benzenediamine, 35 parts of 1,1',1"-[methylidynetris(oxy)]trisethane and 1.5 parts of acetic acid is stirred and refluxed for 2 hours. The reaction mixture is cooled and evaporated. The residue is taken up in 100 parts of water and a hydrochloric acid solution 10 N is added till all solid enters solution. This solution is treated with activated charcoal. The latter is filtered off and the filtrate is alkalized with a sodium hydroxide solution. The product is extracted with dichloromethane. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone. The product is filtered off, washed with a small amount of 4-methyl-2-pentanone and with 2,2'-oxybispropane, and dried, yielding 2.2 parts of 5-[4-(diphenylmethyl)- 1-piperazinylmethyl]-1-propyl-1H-benzimidazole; mp. 154.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04179505 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-103abe9031c04f98b585f1c2fe6aa816 |
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| Source note | uspto-grants-1979_12 |
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