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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379543Generated: October 31, 2026

Acetonitrile → [1-Hydroxy-(E,E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]phosphonic acid

https://huagongshe.com/reaction/2379543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantBromotrimethylsilaneHCID 76113—
ReactantDiethyl [1-hydroxy-(E,E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]phosphonateHCID 15235905—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product[1-Hydroxy-(E,E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]phosphonic acidHCID 15235906—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of diethyl [1-hydroxy-(E,E)-4,8,12-trimethyl-3,7,11-tridecatrienyl]phosphonate (37 mg, 0.0993 mmol) and 2,4,6-collidine (0.052 ml, 0.397 mmol) in dichloromethane (3 ml) under argon at 0° C., was added trimethylsilyl bromide (0.052 ml, 0.397 mmol) and the resulting mixture stirred at 0° C. for 30 min and then at r.t. for 4 hr. The resulting white suspension was diluted with toluene (10 ml) and the solvent evaporated in vacuo. The resulting white solid was dissolved in ethylacetate and water and the pH was adjusted to 3 by the addition of 1M HCl solution. The organic layer was separated and dried (MgSO4) and evaporated to afford a clear oil. Addition of acetonitrile 2 ml precipitated the title compound as an off white solid which was removed by filtration and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362906
Source datasetuspto-grants-1994_11
ORD IDord-5aee9ec29ba54fd7938bae042940861d
Source noteuspto-grants-1994_11