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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409739Generated: October 25, 2026

Tetrapropylammonium → 1-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidin-4-one

https://huagongshe.com/reaction/1409739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrapropylammoniumHCID 9559—
ReactantMethyl morpholine oxideHCID 82029—
Reactant1-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidin-4-OLHCID 21897744—
SolventDichloromethaneHCID 6344—
Product1-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidin-4-oneHCID 66915348—

Reaction Steps

1-[3-(Propan-2-yl)-1,2,4-oxadiazol-5-yl]piperidin-4-ol (0.5 g) is dissolved in dichloromethane (75 mL) and 4 A molecular sieves (4 g) are added followed by N-methylmorpholine-N-oxide (1.52 g) and tetrapropylammonium perrhutenate (0.018 g) and the mixture is stirred at room temperature for 1 h. The reaction is then filtered through celite and the mother liquor washed with water (2×50 mL). The water layers are then combined and back extracted with dichloroemthane (100 mL). The dichloromethane layers are combined, dried over Na2SO4, filtered and concentrated to give the title compound. LC (method 20): tR=1.67 min; Mass spectrum (APCI): m/z=210 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921398B2
Source datasetuspto-grants-2014_12
ORD IDord-38fbc51127124e7badac6fcceb6e2ec6
Source noteuspto-grants-2014_12