HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060193Generated: November 1, 2026
Styrene Oxide → (+/-)-cis-1-[3,5-Bis(trifluoromethyl)benzoyl]-4-[4-(2-hydroxy-2-phenylethyl)-1-piperazinyl]-2-(phenylmethyl)piperidine
https://huagongshe.com/reaction/1060193
Participants
| Role | Name | HCID | Charge |
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| Reactant | Styrene Oxide | HCID 7276 | — |
| Reactant | (+/-)-1-[3,5-Bis(trifluoromethyl)benzoyl]-2-(phenylmethyl)-4-(1-piperazinyl)piperidine | HCID 18630855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (+/-)-cis-1-[3,5-Bis(trifluoromethyl)benzoyl]-4-[4-(2-hydroxy-1-phenylethyl)-1-piperazinyl]-2-(phenylmethyl)piperidine | HCID 15513284 | 7% |
| Product | (+/-)-cis-1-[3,5-Bis(trifluoromethyl)benzoyl]-4-[4-(2-hydroxy-2-phenylethyl)-1-piperazinyl]-2-(phenylmethyl)piperidine | HCID 15513289 | 23% |
Reaction Steps
A mixture of compound 15 (0.005 mol) and 1,2-epoxyethylbenzene (0.006 mol) in methanol (50 ml) was stirred at RT for 1 hour. The mixture was stirred and refluxed for 3 hours. The solvent was evaporated and the residue was purified over silica gel on a glass filter (eluent: CH2Cl2/CH3OH 100/0, 99/1 and 98/2). The pure fractions were collected and the solvent was evaporated. The residue was purified by HPLC over silica gel (eluent: CH2Cl2/CH3OH 98/2 to 95/5). Two pure fractions were collected and their solvents were evaporated. Each residue was dried, yielding 0.7 g (23%) of (±)-cis-1-[3,5-bis(trifluoromethyl)benzoyl]-4-[4-(2-hydroxy-2-phenylethyl)-1-piperazinyl]-2-(phenylmethyl)piperidine (compound 60) and 0.23 g (7%) of (±)-cis-1-[3,5-bis(trifluoromethyl)benzoyl]-4-[4-(2-hydroxy-1-phenylethyl)-1-piperazinyl]-2-(phenylmethyl)piperidine (compound 61).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521621B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-5361b08f459e4acb962b2c5df4649fac |
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| Source note | uspto-grants-2003_02 |
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