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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577491Generated: November 3, 2026

Hydrochloric Acid → HCID 11125018, compound

https://huagongshe.com/reaction/1577491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Ethylhexyl dihydrogen phosphateHCID 14050—
ReactantBis(2-ethylhexyl) phosphorochloridateHCID 173926—
ReactantHCID 178443864HCID 178443864—
SolventWaterHCID 962—
ProductHCID 11125018HCID 11125018—
ProductHCID 178443864HCID 178443864—

Reaction Steps

The final major step in the process of this invention is the hydrolysis of the di-(2-ethylhexyl) phosphorochloridate to product DEHPA. This reaction is carried out using an excess amount of water over the stoichiometric amount. Dealkylation of the DEHPA to mono-(2-ethylhexyl) phosphoric acid by HCl at elevated temperatures is a side reaction that must be controlled to produce acceptable product. This dealkylation is minimized by adjusting the amount of water so that a final HCl content below about 11 wt. % is obtained. In general, the hydrolysis reaction is carried out at 80°-100° C. Considerable amounts (above 60 wt. %) of tetra-(2-ethylhexyl) pyrophosphate are formed in this process from the reaction of DEHPC with DEHPA. This lowers product purity and causes processing problems, such as poorer phase separation. This is overcome by extending the hydrolysis time to 4-6 hours to hydrolyze the pyrophosphate to DEHPA product. An alternative and preferred method to carry out the hydrolysis is to hydrolyze the mixture, as above described for about 2 hours at about 80° C. Then the aqueous layer containing the HCl is separated. A second hydrolysis, using the same amount of water as previously stated, is carried out at 95°-100° C. for about 3 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04288392
Source datasetuspto-grants-1981_09
ORD IDord-60c511417eed442ebcd7f2a5706018b4
Source noteuspto-grants-1981_09