HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172185Generated: October 30, 2026
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → HCID 67275611, compound
https://huagongshe.com/reaction/2172185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 70873872 | HCID 70873872 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67275611 | HCID 67275611 | 73.9% |
Reaction Steps
Pyridinium p-toluenesulfonate (81 mg) was added to an ethanol solution (3 ml) of 1-[4-(tetrahydropyran-2-yloxy)phenyl]-4-(4-trifluoromethoxybenzyloxy)piperidine (507 mg) and the mixture was stirred at 70 to 80° C. for 24 hours. After being cooled to room temperature, the reaction mixture was concentrated under reduced pressure, ethyl acetate and a saturated sodium hydrogen carbonate aqueous solution were added to the residue, and the result was separated into layers. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over magnesium sulfate. After being concentrated under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to afford the title compound as a pale purple solid (305 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051333B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-a9878beff5584fe387fa49e7290ba246 |
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| Source note | uspto-grants-2015_06 |
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