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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379539Generated: October 30, 2026

2,4,6-Trimethylpyridine → HCID 18957432, compound

https://huagongshe.com/reaction/2379539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantBromotrimethylsilaneHCID 76113—
ReactantHCID 21756367HCID 21756367—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 18957432HCID 18957432—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of dimethyl[1-hydroxy-(E,E)-5,9,13-trimethyl-4,8,12-tetradecatrienyl]phosphonate (98 mg, 0.253 mmol) and 2,4,6-collidine (0.134 ml, 1.014 mmol) in dichloromethane (3 ml) under arson at 0° C., was added trimethylsilyl bromide (0.134 ml, 1.013 mmol) and the resulting mixture stirred at 0° C. for 30 min. and then at r.t. for 5 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, dried (Na2SO4) and evaporated to afford a glassy residue. The solid was washed with acetonitrile (2×5 ml) and the white solid filtered off and dried in vacuo to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05362906
Source datasetuspto-grants-1994_11
ORD IDord-7f67b3e5a05b400eb1bc656baf5acdf4
Source noteuspto-grants-1994_11