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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257675Generated: October 30, 2026

Dodecanoyl chloride → 2,6-Diphenyl-4-piperidyl laurate

https://huagongshe.com/reaction/257675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecanoyl chlorideHCID 8166—
Reactant2,6-Diphenylpiperidin-4-olHCID 13068932—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2,6-Diphenyl-4-piperidyl laurateHCID 1525048474.2%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a -70° C. solution of 2.50 g (9.9 mmol) of 2,6-diphenyl-4-hydroxypiperidine in 80 ml of dry tetrahydrofuran (THF), 4.2 mL (10.5 mmol) of n-butyllithium (2.5M in hexanes) is added dropwise. The mixture is warmed to -20° C. and stirred for 30 minutes. The solution is then cooled again to -70° C. and a solution of 2.2 g (9.9 mmol) of lauroyl chloride in 20 mL of dry THF is then added dropwise. The mixture is warmed to room temperature and stirred for 18 hours. The mixture is added to 250 mL of brine and then extracted with 2×200 mL of ether. The combined organic layers are dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue is purified by liquid chromatography (LC) (silica gel, ethyl acetate/hexane) to give 3.2 g (74%) of the title compound as a white solid: mp 40°-42° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262538
Source datasetuspto-grants-1993_11
ORD IDord-9e1cd3c8aa644f8aa87c8f8dc36ca49e
Source noteuspto-grants-1993_11