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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345490Generated: October 29, 2026

Oxalic Acid → HCID 86745166, compound

https://huagongshe.com/reaction/345490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 5106095HCID 5106095—
ReactantBis(4-fluorophenyl)(piperidin-4-yl)methanolHCID 11208889—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86745166HCID 8674516626%

Reaction Steps

A mixture of 6.1 g (0.020 mole) of α,α-bis(4-fluorophenyl)-4-piperidinemethanol, 4.8 g (0.024 mole) of 4-chloro-N-phenylbutanamide, 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 L of water and extracted thrice with 100 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 250 g of silica gel on a 65 cm×4 cm column, eluted with 10% methanol in methylene chloride. The fractions containing the desired product were combined and concentrated under reduced pressure to give a foam. The foam was converted to the oxalic acid salt, and the solid was recrystallized from 2-propanol to yield 3.0 g (26 %) of the title compound as a white solid, mp 145°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057524
Source datasetuspto-grants-1991_10
ORD IDord-7620f6739af74f6d8c518f172b705142
Source noteuspto-grants-1991_10