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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345489Generated: October 29, 2026

Oxalic Acid → HCID 86745165, compound

https://huagongshe.com/reaction/345489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant4-chloro-N,N-dimethylbutyramideHCID 89852—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86745165HCID 8674516516%

Reaction Steps

A mixture of 6.1 g (0.020 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 3.7 g (0.025 mole) of 4-chloro-N,N-dimethylbutanamide, 8.5 g (0.080 mole) of anhydrous sodium carbonate and 0.3 g (0.002 mole) of potassium iodide in 100 mL of N,N-dimethylformamide was heated on a steam bath for 16 h. The mixture was poured into 1.5 L of water and extracted thrice with 500 mL portions of ethyl acetate. The ethyl acetate fractions were combined, washed with water and brine, dried (MgSO4), and concentrated under reduced pressure to give a viscous oil. The oil was purified by column chromatography using 300 g of silica gel on a 65 cm×4 cm column, eluted with methanol-methylene chloride (1:15). Fractions containing the desired product were combined and concentrated under reduced pressure to give a viscous oil. The oil was converted to the oxalic acid salt and the solid was recrystallized from 2-propanol/ethyl acetate to yield 1.6 g (16%) of the title compound as a white solid, mp 156°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057524
Source datasetuspto-grants-1991_10
ORD IDord-91ec7ce62862458a85881eb6c3203a16
Source noteuspto-grants-1991_10