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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantAmmonium ChlorideHCID 25517—
Reactant(10-Undecenyl)phosphono chloridic acid, ethyl esterHCID 21054114—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product((10-Undecenyl)-ethoxyphosphinyl)methylphosphonic acid dimethyl esterHCID 2105411778%

Reaction Conditions

Temperature-50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754200B2
Source datasetuspto-grants-2010_07
ORD IDord-b6a6601c3bff46d49a9361dd549fa1da
Source noteuspto-grants-2010_07