HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354493Generated: October 31, 2026
Hexane → ((10-Undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl ester
https://huagongshe.com/reaction/2354493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (10-Undecenyl)phosphono chloridic acid, ethyl ester | HCID 21054114 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ((10-Undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl ester | HCID 21054117 | 78% |
Reaction Steps
A 2.5 M solution of n-butyllithium in hexane (9.4 mL, 23.5 mmol) was added dropwise with stirring to methylphosphonic acid dimethyl ester (2.65 g, 21.4 mmol) in 100 mL of anhydrous tetrahydrofuran at −78° C. under a nitrogen atmosphere. After 30 minutes, (10-undecenyl)phosphono chloridic acid, ethyl ester (3 g, 10.68 mmol) was added dropwise while stirring was continued. The reaction was stirred at −78° C. for 2 hours then warmed to −50° C. and stirred for an additional 2 hours. Saturated ammonium chloride was then added to neutralize the excess base and the reaction was allowed to warm to ambient temperature. The volatiles were removed by rotary evaporation to give a viscous liquid. This liquid was diluted with ethyl acetate (200 mL) and extracted twice with water (100 mL). The organic layer was collected and dried over sodium sulfate, filtered and concentrated under rotary evaporation to give a viscous liquid. The product was then placed on a high vacuum pump to remove any remaining volatiles (3.07 g, 78% 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-b6a6601c3bff46d49a9361dd549fa1da |
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| Source note | uspto-grants-2010_07 |
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