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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9516Generated: October 26, 2026

Hydrogen Peroxide → HCID 178418940, compound

https://huagongshe.com/reaction/9516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant1-OcteneHCID 8125—
ReactantHCID 178418950HCID 178418950—
SolventEthanolHCID 702—
SolventSulfuric AcidHCID 1118—
ProductHCID 178418940HCID 17841894084.8%

Reaction Steps

To a mixture of 95.1 g (0.897 mol) of sodium hypophosphite hydrate in 600 mL 95% ethanol, 23.8 mL of concentrated sulfuric acid was added. 1-Octene (33.6 g, 0.299 mol) was added to the stirred mixture followed by 1.69 g (0.0149 mol) of 30% hydrogen peroxide. The resulting mixture was refluxed for 8 hs, and then another 1.15 g (0.010 mol) of hydrogen peroxide was added and the reaction mixture was continued to reflux for another 8 hs. The resulting mixture was cooled, filtered, and then the ethanol was removed using a rotary evaporator. To the resulting residue, 200 mL water was added and then 50% sodium hydroxide solution was added until the solution became alkaline. The mixture was extracted twice with 200 mL diethyl ether, and the aqueous phase was then acidified with concentrated sulfuric acid. The aqueous layer was extracted with 200 mL ethyl acetate, and the organic layer was washed with saturated sodium chloride and then dried over anhydrous magnesium sulfate. The organic layer was decanted and the drying agent was washed with another 50 mL ethyl acetate. The combined organic layers were evaporated on a rotary evaporator. 45.2 g of n-octylphosphinic acid (84.8% yield) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091262B2
Source datasetuspto-grants-2006_08
ORD IDord-2a9a67b66c664cd1a09355b567f720a0
Source noteuspto-grants-2006_08