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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927444Generated: November 3, 2026

Potassium Carbonate → Ethyl E-8-[2-(4-tert-butylbenzyloxy)phenyl]-6-(4-cyanobenzyl)oct-7-enoate

https://huagongshe.com/reaction/1927444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
ReactantEthyl E-6-(4-cyanobenzyl)-8-(2-hydroxyphenyl)oct-7-enoateHCID 57831344—
SolventAcetonitrileHCID 6342—
ProductEthyl E-8-[2-(4-tert-butylbenzyloxy)phenyl]-6-(4-cyanobenzyl)oct-7-enoateHCID 57831393—

Reaction Steps

A solution of 1.75 g (4.64 mmol) of ethyl E-6-(4-cyanobenzyl)-8-(2-hydroxyphenyl)oct-7-enoate in 50 ml of dry acetonitrile is mixed with 1579 mg (6.95 mmol) of 4-(tert-butyl)benzyl bromide and 961 mg (6.95 mmol) of anhydrous potassium carbonate and heated under reflux for 12 hours. The mixture is then concentrated to dryness. The residue is taken up in ethyl acetate, washed with water and saturated sodium chloride solution and dried over sodium sulfate. The organic phase is concentrated. The resulting crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 8:1→4:1). 2.24 g (4.28 mmol, 92% of theory) of a solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183271B2
Source datasetuspto-grants-2012_05
ORD IDord-4e6d4db233a84338a3185e90ceb811d4
Source noteuspto-grants-2012_05