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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501783Generated: October 30, 2026

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

https://huagongshe.com/reaction/501783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactant2-(2-Methylpropoxy)benzaldehydeHCID 3857528—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productethyl (E)-3-(2-isobutoxyphenyl)-2-propenoateHCID 17816555—

Reaction Conditions

Temperature40 °C

Reaction Steps

0.92 g of 60% sodium hydride was suspended in 30 mL of tetrahydrofuran, to which 5.0 mL of ethyl diethylphosphonoacetate was added dropwise over 5 minutes at room temperature, and this mixture was stirred for 30 minutes at 40° C. Then, after 3.40 g of 2-isobutoxybenzaldehyde dissolved in 20 mL of tetrahydrofuran was added to the mixture dropwise over 20 minutes at room temperature, this mixture was stirred for one hour at the same temperature. The reaction mixture was added to a mixture of ethyl acetate and water, and the organic phase was separated therefrom. After the resultant organic phase was washed with water and a saturated sodium chloride solution successively, the washed phase was dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure. The resultant residue was purified by silica gel column chromatography [eluent; hexane:ethyl acetate=9:1] to yield 4.30 g of ethyl (E)-3-(2-isobutoxyphenyl)-2-propenoate as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772285B2
Source datasetuspto-grants-2010_08
ORD IDord-bed8a0197ac0425d8d5f85497bb55ed4
Source noteuspto-grants-2010_08