HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354494Generated: October 31, 2026
Acetone → ((10-Undecenyl)-hydroxyphosphinyl)methylphosphonic acid tri sodium salt
https://huagongshe.com/reaction/2354494
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | ((10-Undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl ester | HCID 21054117 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ((10-Undecenyl)-hydroxyphosphinyl)methylphosphonic acid tri sodium salt | HCID 131725942 | 74% |
Reaction Steps
Bromotrimethylsilane (0.8 mL, 6.06 mmol) was added dropwise to ((10-undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl ester (0.250 g, 0.68 mmol) in a 3 mL vial. This solution was stirred for 14-16 hours at ambient temperature. Excess bromotrimethylsilane was removed by passing a steady stream of dry nitrogen over the solution for 2 hours. The residue was then placed under high vacuum for 3 hours to remove residual bromotrimethylsilane. Tributylamine (0.57 g, 3.08 mmol) and methanol (3 mL) was then added to the residue resulting in a clear solution. This mixture was added dropwise to a 0.5 M solution of NaI in acetone (10 mL, 5.0 mmol). A white solid precipitated immediately. The solid was collected by centrifugation and the acetone solution was discarded. The solid was then washed by suspension in clean acetone (20 mL), centrifugation and removal of acetone supernatant. After this washing procedure was completed 3 times, the solid was placed under vacuum for a period of 12-16 hours providing the desired product (0.19 g, 74% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754200B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-ae7e33db8c924605b4d9899eaa31a78e |
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| Source note | uspto-grants-2010_07 |
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