Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023838Generated: November 2, 2026

4-Piperidineethanol → HCID 67206122, compound

https://huagongshe.com/reaction/1023838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidineethanolHCID 73953—
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductHCID 67206122HCID 6720612245%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(piperidin-4-yl)ethanol (0.30 g, 2.32 mmol) in anhydrous dichloromethane (10 mL), NaHCO3 (0.59 g, 6.97 mmol) was added. The suspension was cooled to 0° C. and then 3,3-dimethylbutanoyl chloride (0.38 g, 2.79 mmol) was added dropwise over a period of 15 min. The reaction was followed by TLC till the disappearance of the starting material (overnight) and was then filtered. The residue was then purified using column chromatography on a silica gel column eluting with a solution of ethyl acetate in hexane (50%) to produce the alcohol in a 45% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722720B2
Source datasetuspto-grants-2014_05
ORD IDord-daa69363e0594b118ec804e3dc912eef
Source noteuspto-grants-2014_05