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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760968Generated: October 31, 2026

1-Iodopropane → 1-Propylpiperidin-4-ol

https://huagongshe.com/reaction/1760968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
ReactantPiperidin-4-olHCID 79341—
SolventAcetoneHCID 180—
Product1-Propylpiperidin-4-olHCID 13665269—

Reaction Steps

1-Iodopropane (22 ml) was added dropwise during 15 minutes to a stirred suspension of 4-hydroxypiperidine (20 g) in acetone (250 ml) and the resultant mixture was stirred at ambient temperature for 20 hours. The mixture was evaporated and the residue was partitioned between diethyl ether and 2N aqueous sodium hydroxide solution. The organic phase was washed with brine, dried over magnesium sulphate and evaporated to give 4-hydroxy-N-propylpiperidine as an oil (19.6 g); NMR Spectrum: (DMSOd6) 0.82 (t, 3H), 1.16 (m, 4H), 1.66 (m, 2H), 1.91 (m, 2H), 2.06 (t, 2H), 2.64 (m, 2H), 3.38 (m, 1H), 4.45 (d, 1H); Mass Spectrum: M+H+ 144.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846827B1
Source datasetuspto-grants-2005_01
ORD IDord-cc68eb2293d64394bf31adfbe3250c66
Source noteuspto-grants-2005_01