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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954122Generated: November 3, 2026

Water → HCID 23295884, compound

https://huagongshe.com/reaction/1954122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-PiperidoneHCID 12665—
ReactantPotassium HydroxideHCID 14797—
Reactant11-Bromo-1-undeceneHCID 284148—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23295884HCID 2329588446%

Reaction Steps

This example illustrates a synthesis of N-(10,11-Oxidoundecyl)-2-piperidone (inventive compound no. 1618). A mixture of potassium hydroxide (1.55 g, 25 mmol, pellets ground in mortar and pestle) and tetrabutylammonium bromide (1.61 g, 5.0 mmol) was stirred in dry tetrahydrofuran (10 mL). A solution of d-valerolactam (2.5 g, 25 mmol) and 1-bromo-10-undecene (Lancaster, 5.9 g, 25 mmol) in tetrahydrofuran (15 mL) was added by syringe pump over 1 hour. After stirring for a further 6 hours. Water (60 mL) and dichloromethane (60 mL) was added to the reaction mixture. The layers were separated and the aqueous layer was extracted with dichloromethane (2×50 mL). The combined organic layers were washed with water (50 mL) and saturated salt solution (50 mL) and then dried with sodium sulfate. The residue was further purified by chromatography using silica and 30% hexane, ethyl acetate to yield 2.88 g (46% yield) of N-(10-Undecenyl)-2-piperidone (inventive compound no. 1616) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121270
Source datasetuspto-grants-2000_09
ORD IDord-8dbc2b8dd2894997b89f2cc8ba552c95
Source noteuspto-grants-2000_09