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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,2-HexadecanediolHCID 98037—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2,6-Di(phenyl)-4-piperidoneHCID 2828708—
SolventTolueneHCID 1140—
Product2,6-Diphenyl-4-piperidone 1,2-Hexadecylene KetalHCID 8674710038.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05235056
Source datasetuspto-grants-1993_08
ORD IDord-2febec4c3e434ed3964f3f9c334d127c
Source noteuspto-grants-1993_08