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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071416Generated: November 3, 2026

Sodium Acetate → Oxalic acid--4-(1-benzylpiperidin-3-yl)-1,2-phenylene diacetate (1/1)

https://huagongshe.com/reaction/2071416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantHCID 20370845HCID 20370845—
SolventAcetic AnhydrideHCID 7918—
ProductOxalic acid--4-(1-benzylpiperidin-3-yl)-1,2-phenylene diacetate (1/1)HCID 3046215224.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

9.8 g of anhydrous sodium acetate were added to a mixture of 9.8 g of the product of Step B and 120 ml of acetic acid anhydride and the mixture was stirred at 20° C. for 3 hours and was then filtered. The filter was washed with ethanol and the filtrate was evaporated to dryness under reduced pressure. The residue was taken up in water and ethyl acetate and the solution was made alkaline with an aqueous solution saturated with sodium bicarbonate. The ethyl acetate phase was recovered by decanting, was dried and evaporated to dryness. The residue was dissolved in 50 ml of isopropanol and a solution of 4 g of oxalic acid in 50 ml of isopropanol was added thereto. The mixture was refluxed until dissolution occurred and was cooled to 20° C. and vacuum filtered to obtain 13.5 g of N-benzyl-3-(3',4'-diacetoxyphenyl)-piperidine oxalate melting at 145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046901
Source datasetuspto-grants-1977_09
ORD IDord-e6122870b25a4837b16948fac292b706
Source noteuspto-grants-1977_09