HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461645Generated: October 29, 2026
Lauryl alcohol ethylene oxide → Oleylmethyldihydroxyethylammonium laurylethoxyethyl phosphate
https://huagongshe.com/reaction/1461645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lauryl alcohol ethylene oxide | HCID 14122790 | — |
| Reactant | Oleylmethyldihydroxyethylammonium chloride | HCID 86745345 | — |
| Reactant | Potassium monolaurylethoxyethyl phosphate | HCID 87761845 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Oleylmethyldihydroxyethylammonium laurylethoxyethyl phosphate | HCID 131717135 | 96.8% |
Reaction Steps
A four-necked flask fitted with stirrer and condenser means was charged with 40.5 g of oleylmethyldihydroxyethylammonium chloride, 21.5 g of potassium monolaurylethoxyethyl phosphate prepared from lauryl alcohol-ethylene oxide (2 mol) adduct and 150 g of isopropyl alcohol and the reaction was conducted at 75°-80° C. in an atmosphere of nitrogen gas introduced at a low flow rate for 8 hours. The precipitate was then collected by filtration and washed with 50 ml of isopropyl alcohol. The filtrate and the washings were combined and concentrated under reduced pressure and the residue was dissolved in 200 g of benzene and filtered. The filtrate was then concentrated to give 51.27 g (theoretical yield 54.55 g) of oleylmethyldihydroxyethylammonium laurylethoxyethyl phosphate as a waxy product. The elemental analysis is shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05076828 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-80658ef5b4b94f20a7ce708a1c44e382 |
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| Source note | uspto-grants-1991_12 |
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