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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602851Generated: October 27, 2026

Cyclohexane → Lanthanum di(2-ethylhexyl) phosphate

https://huagongshe.com/reaction/602851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantLanthanum sesquioxideHCID 150906—
ReactantBis-(2-ethylhexyl) phosphateHCID 15302585—
SolventWaterHCID 962—
ProductLanthanum di(2-ethylhexyl) phosphateHCID 18461867—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a four neck flask of 200 ml are added 3.26 g (10 mmol) of lanthanum oxide, 19.94 g (60 mmol) of di(2-ethylhexyl) phosphate [Starting Material A] and 85 g of cyclohexane at 20° C. and then 3.33 g of water is added, which are agitated and heated to raise a temperature of a reaction solution to 50° C. Although the agitation is continued at this temperature for 4 hours, the reaction solution becomes whitely clouded. The temperature of the reaction solution is made to 70° C. by gradually heating, and further the agitation is continued at this temperature for 20 hours, but unreacted lanthanum oxide is still alive and the reaction is not completed. The reaction solution is filtered to recover 0.85 g of the unreacted lanthanum oxide. The filtrate is returned to the four neck flask and a reflux dehydrator is mounted thereonto to remove water in the filtrate through azeotropy with cyclohexane to obtain a solution of lanthanum di(2-ethylhexyl) phosphate in hexane. Further, hexane is distilled off under a reduced pressure to obtain 53.5 g of a solution of lanthanum di(2-ethylhexyl) phosphate in hexane having a concentration of about 40%. The analytical results are shown in Table 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906631B2
Source datasetuspto-grants-2011_03
ORD IDord-1fb88c629e9b44f6a06aabbd3e98a087
Source noteuspto-grants-2011_03