Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12136656 | HCID 12136656 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12136657 | HCID 12136657 | 88.5% |
Reaction Steps
To a suspension of 1-{4-[5-(4-chloro-benzenesulfonyl)2-methoxyphenyl]piperidin-1-yl}-2,2,2-trifluoro-ethanone (31) (77 mg) in methanol (2 mL), a solution of 6N NaOH (0.5 mL) was added. After stirring at 80° C. for 10 min, water was added (10 ml) and the mixture was extracted into ethyl acetate (20 ml). The organic phase was dried (Na2SO4) and concentrated in vacuo to give 4-[5-(4-chloro-benzenesulfonyl)2methoxy-phenyl] piperidine (301) as a white solid (0.054 g ), MS, MH+ 365. The hydrochloride salt was prepared from ethanol-hydrogen chloride, m.p. 235.5-236.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825202B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-28885d7c0e984811aa161152fd130638 |
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| Source note | uspto-grants-2004_11 |
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