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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488169Generated: October 29, 2026

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

https://huagongshe.com/reaction/488169

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 numberUS05298655
Source datasetuspto-grants-1994_03
ORD IDord-7de4d7ca9fa44203b0f1ae98a3b46fb2
Source noteuspto-grants-1994_03