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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249671Generated: October 29, 2026

Ethyl Acetate → Ethyl 3-(2-isobutoxyphenyl)-2-propenoate

https://huagongshe.com/reaction/2249671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactant2-(2-Methylpropoxy)benzaldehydeHCID 3857528—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(2-isobutoxyphenyl)-2-propenoateHCID 68983960—

Reaction Conditions

Temperature40 °C

Reaction Steps

In 30 ml of tetrahydrofuran is suspended 0.92 g of 60% sodium hydride. After dropping 5.0 ml of ethyl diethylphosphonoacetate thereinto at ambient temperature over a period of 5 minutes, the mixture thus obtained is stirred at 40° C. for 30 minutes. Then, a solution of 3.40 g of 2-isobutoxybenzaldehyde in 20 ml of tetrahydrofuran is dropwise added at ambient temperature over a period of 20 minutes, and the mixture thus obtained is stirred for one hour. The reaction mixture is added to a mixture of ethyl acetate and water, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=9:1) to obtain 4.30 g of ethyl 3-(2-isobutoxyphenyl)-2-propenoate as a light yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-bd1a93d8e8914827a2526eb9400828ab
Source noteuspto-grants-2008_01