HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254393Generated: October 25, 2026
Water → 2,6-Diphenyl-4-piperidone 1,2-Hexadecylene Ketal
https://huagongshe.com/reaction/2254393
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Hexadecanediol | HCID 98037 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2,6-Di(phenyl)-4-piperidone | HCID 2828708 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Diphenyl-4-piperidone 1,2-Hexadecylene Ketal | HCID 86747100 | 38.6% |
Reaction Steps
A solution of 14.6 g (58.0 mmol) of 2,6-diphenyl-4-piperidone and 12.2 g (64 mmol) of p-toluenesulfonic acid monohydrate in 500 mL of toluene is refluxed and the azeotroping water is collected in a Dean Stark trap. When 1 mL of water is collected, 15.0 g (58.0 mmol) of 1,2-hexadecanediol (Aldrich) is added and the reaction is refluxed until another 1 mL of water is collected. The reaction mixture is cooled to room temperature and made basic with 50% aqueous sodium hydroxide solution. The organic layer is separated and the aqueous phase is extracted with toluene (2×100 mL). The combined organic phases are dried over anhydrous magnesium sulfate and the solvent is removed under reduced pressure. 11.0 g (38% yield) of the title compound is isolated after purification by liquid chromatography (LC) (silica gel, ethyl acetate/hexane) followed by recrystallization from ethanol: mp 63°-70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05235056 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-2febec4c3e434ed3964f3f9c334d127c |
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| Source note | uspto-grants-1993_08 |
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