Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 131731753 | HCID 131731753 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 57964197 | HCID 57964197 | 50% |
Reaction Steps
A suspension of 0.41 g (1 mmol) of 1-(2,3-dichlorophenyl)-4-(2-piperidin-4-ylethyl)piperazine, dihydrochloride in 25 mL of isopropanol and 0.29 g (2.1 mmol) of potassium carbonate is stirred for 30 minutes then 0.08 g (1.1 mmol of 2-ethyloxirane is added. The suspension is stirred to reflux overnight. The precipitate is filtered and the solution is concentrated under reduced pressure. The residue is dissolved in ethyl acetate, washed with water and with brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue is purified over 10 g of silica gel (dichloromethane/methanol 90/10) to give 0.2 g (50%) of 1-(4-{2-[4-(2,3-dichlorophenyl)piperazin-1-yl]ethyl}piperidin-1-yl)butan-2-ol as an oil that crystallizes upon standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802678B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-c743d9e54a6148f29b1287c7efb39058 |
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| Source note | uspto-grants-2014_08 |
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