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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920580Generated: October 30, 2026

Potassium Carbonate → Methyl 4-((4E)-5-{2-[(4-tert-butylbenzyl)oxy]phenyl}-3-{2-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]-ethyl}pent-4-en-1-yl)benzoate

https://huagongshe.com/reaction/1920580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
ReactantMethyl 4-[(4E)-3-{2-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]ethyl}-5-(2-hydroxyphenyl)pent-4-en-1-yl]benzoateHCID 57965770—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-((4E)-5-{2-[(4-tert-butylbenzyl)oxy]phenyl}-3-{2-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]-ethyl}pent-4-en-1-yl)benzoateHCID 57965760—

Reaction Steps

134.6 mg (0.59 mmol) of 4-(tert-butyl)benzyl bromide and 163.8 mg (1.18 mmol) of anhydrous potassium carbonate are added to a solution of 178 mg (0.395 mmol) of methyl 4-[(4E)-3-{2-[1-(2-ethoxy-2-oxoethyl)cyclopropyl]ethyl}-5-(2-hydroxyphenyl)pent-4-en-1-yl]benzoate in 5 ml of dry acetonitrile, and the mixture is 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 crude product obtained is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 10:1). This gives 130.6 mg (55% of theory) of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168821B2
Source datasetuspto-grants-2012_05
ORD IDord-223901bad6a7488cbe691d428666bd0f
Source noteuspto-grants-2012_05