Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410089Generated: October 26, 2026

Oxalic Acid → 2-Oxa-6-azaspiro(3.3)heptane hemioxalate

https://huagongshe.com/reaction/1410089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
ReactantSodium SulfateHCID 24436—
ReactantSodium sulfate decahydrateHCID 62649—
ReactantMagnesiumHCID 5462224—
Reactant6-Tosyl-2-oxa-6-azaspiro[3.3]heptaneHCID 23319891—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Product2-Oxa-6-azaspiro(3.3)heptane hemioxalateHCID 5459444248.6%

Reaction Steps

6-(Toluene-4-sulfonyl)-2-oxa-6-azaspiro[3.3]heptane (510 mg, 2 mmol) and magnesium granular (336 mg, 14 mmol) were sonicated for one hour in methanol (100 ml). Almost all solvent was removed from the grey reaction mixture on a rotary evaporator to give a viscous grey residue. Diethyl ether (10 ml) and sodium sulfate decahydrate (1 g) were added and the resulting light grey mixture was stirred vigorously for 30 minutes before filtration. The filtrate was dried over anhydrous sodium sulfate and anhydrous oxalic acid (90 mg, 1 mmol) dissolved in Ethanol (˜0.5 mL) was added to the organic phase. A thick white precipitate formed instantly. It was filtered off and dried under vacuum to give 2-oxa-6-azaspiro[3.3]heptane hemioxalate (140 mg, 37%) off-white solid. 1H NMR (300 MHz, CDCl3) δ 4.64 (s, 4H), 4.11 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921383B2
Source datasetuspto-grants-2014_12
ORD IDord-3c7d69d300d24b5597632f3b12fba562
Source noteuspto-grants-2014_12