Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410494Generated: November 2, 2026

Ethanol → 4-(Propan-2-yl)-1,4-azaphosphinane 4-oxide oxalate salt

https://huagongshe.com/reaction/410494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantOxalic acid dihydrateHCID 61373—
Reactant1-Benzyl-4-(propan-2-yl)-1,4-azaphosphinane 4-oxideHCID 67432951—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
Product4-(Propan-2-yl)-1,4-azaphosphinane 4-oxide oxalate saltHCID 6743025053%

Reaction Steps

A 10 L auto clave was charged with the product of Step 2 (200.0 g, 796.8 mmol), ethanol (4000 mL) and oxalic acid dihydrate (100.4 g, 797.0 mmol) in water (1000 ml). To the reaction mixture was added palladium on carbon (10% w/w, 99.6 g) and stirred at room temperature under H2 pressure (50 psi) for 16 h. After completion, the reaction mixture filtered and concentrated. Obtained solid was triturated with hot ethanol (250 mL) and kept in a cold room for 90 minutes, filtered, washed with diethylether and hexane to give 4-(propan-2-yl)-1,4-azaphosphinane 4-oxide oxalate salt (105 g, 53%) as a colorless solid. Mp 223-224° C. LC ESI: [M]+ m/z 162. HPLC (ELSD method)=99.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-6a0be3fccb4e4d53ad0e05673f99fe70
Source noteuspto-grants-2014_06