HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577346Generated: October 26, 2026
Hydrochloric Acid → N-Benzyl-3-acetoxy-3-(m-trifluoromethylphenyl)piperidine hydrochloride
https://huagongshe.com/reaction/1577346
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzyl-3-(3-trifluoromethyl-phenyl)-piperidine-3-ol | HCID 20506415 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Benzyl-3-acetoxy-3-(m-trifluoromethylphenyl)piperidine hydrochloride | HCID 20506441 | — |
Reaction Steps
A mixture of 37 g. of N-benzyl-3-hydroxy-3-(m-trifluoromethylphenyl)piperidine, 220 ml. of acetic anhydride and 0.3 ml. of concentrated sulfuric acid is heated to 110° C. for one hour. After cooling it is poured onto ice-water, the resulting mixture agitated for 15 minutes and made alkaline by addition of sodium hydroxide solution. The mixture is extracted with ethyl acetate, the extracts washed with brine, dried (MgSO4) and evaporated to dryness to obtain 39 g. of the free base. This is dissolved in 600 ml. of ethyl acetate, cooled in ice, and 100 ml. of ethanol saturated with hydrogen chloride is added. The solvent is removed by evaporation in vacuo and the residue triturated with 200 ml. of ethyl acetate then 200 ml. of ethyl ether is added and the mixture allowed to stand overnight. The crystalline title compounds is collected by filtration, washed with ether and dried to obtain 36 g., M.P. 206°-207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04287341 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-cc26fec3350d4cefbb98297945c1710f |
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| Source note | uspto-grants-1981_09 |
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