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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433237Generated: October 30, 2026

Imidazole → (E)-ethyl 7-(tert-butyldimethylsiloxy)-2-methyl-2-heptenate

https://huagongshe.com/reaction/1433237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDichloromethaneHCID 6344—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(E)-ethyl 7-hydroxy-2-methyl-2-heptenateHCID 10559469—
SolventDimethylformamideHCID 6228—
Product(E)-ethyl 7-(tert-butyldimethylsiloxy)-2-methyl-2-heptenateHCID 1105570498.8%

Reaction Steps

To a methylene chloride solution (300 ml) of Ester 3 (13.91 g; 0.0748 mol), 43 ml of DMF (dimethylformamide) and imidazole (7.6 g; 0.112 mol) are added and the whole is stirred until imidazole is fully dissolved. Tert-butyldimethylsilyl chloride (13.5 g; 0.0897 mol) is then added thereto and the whole is stirred for 20 min. After stirring, the resultant solution is quenched using a buffer solution (100 ml) and the organic compound is extracted three times with ethyl acetate, followed by the wash of the organic layer in a saturated saline solution and drying over anhydrous magnesium sulfate. After anhydrous magnesium sulfate is filtered and the solvent is distilled off under reduced pressure, the residue is separated and purified by column chromatography (developing solution, ethyl acetate:hexane=1:1) to produce Ester 4 (22.16 g; 0.0739 mol) of 99% in yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612213B2
Source datasetuspto-grants-2009_11
ORD IDord-3b9799b2bfdd4e4a82e648bd255e920b
Source noteuspto-grants-2009_11