Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | Ethyl 2-[4-(2-(4-(1-(2-ethoxyethyl)benzimidazole-2-yl)piperidine-1-yl)ethyl)phenyl]-2-methylpropanoate | HCID 66869688 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69154773 | HCID 69154773 | 54.7% |
Reaction Steps
1 g of aluminium and lithium hydride was dissolved in 30 ml of THF and 3 g of ethyl 2-[4-(2-(4-(1-(2-ethoxyethyl)benzimidazole-2-yl)piperidine-1-yl)ethyl)phenyl]-2-methylpropanoate were added dropwise thereto. This was stirred for four hours at room temperature and some milliliters of water were added to eliminate excess hydride. The solution was filtered and the filtrate was washed with a saturated sodium chloride solution. This was dried and concentrated. The residue was redissolved in chloroform and washed with water, dried and concentrated. The residue was purified by flash-chromatography using a hexane/ether/isopropyl-amine mixture (2/7.5/0.5) as an eluent, to yield 1.5 g of 1-(2-ethoxyethyl)-2-[1-(2-(4-(1,1-dimethyl-2-hydroxyethyl)phenyl)ethyl)piperidine-4-yl]-1H-benzimidazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05877187 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-2ee53132c2cb46e0931b9022faefd13c |
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| Source note | uspto-grants-1999_03 |
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