Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67770164 | HCID 67770164 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 23362149 | HCID 23362149 | 100.4% |
Reaction Steps
To a solution containing 1.2 g (0.03 mol) of sodium hydroxide in 50 ml of an 50% by volume ethanol/water mixture, 12.41 g (0.03 mol) of 1-(4-chlorophenyl)-3-[4-hydroxy-(4-chlorophenyl)-1-piperidyl]propanone hydrochloride and then, over 1 hour 1.17 g of sodium borohydride are added. The suspension is heated at a temperature of 50° C. for 2 hours. After cooling down, the reaction mixture is filtered and washed with water to give 11.45 g of product, m.p.: 129°-132° C. After recrystallization of the latter product from 215 ml of acetonitrile, 9.1 g of title compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05589486 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-6f520badb0e446cbaf35cbd7717452cd |
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| Source note | uspto-grants-1996_12 |
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