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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680430Generated: October 29, 2026

Ethanol → HCID 12944322, compound

https://huagongshe.com/reaction/1680430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalic AcidHCID 971—
ReactantHCID 131712079HCID 131712079—
ProductHCID 12944322HCID 12944322—

Reaction Steps

3-[(4-Hydroxypiperidino)methyl]-4-(4-(hydroxypiperidino)butan-2-one (1 g.) was dissolved in 8 ml. of ethyl alcohol and added to a cooled solution of oxalic acid anhydrous (0.9 g.) in 5 ml. of ethyl alcohol. After standing at 0° C. for five minutes, the resultant precipitate was filtered. The filtrate was stripped of solvent under reduced pressure and the residual oil taken up in a small volume of water, saturated with potassium carbonate and then extracted with ether. The ether solution was dried over anhydrous sodium sulphate, filtered and the filtrate stripped of ether. The residual oil, approximately 0.1 g., was characterized including a proton nuclear magnetic resonance spectrum in deuterated dimethylsulfoxide. There were two vinylic protons, at 5.9 and 6.1 ppm downfield from the reference tetramethylsilane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273781
Source datasetuspto-grants-1981_06
ORD IDord-fa01a19570eb482cbaf6d140551a3693
Source noteuspto-grants-1981_06