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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249637Generated: November 2, 2026

Hydrochloric Acid → Ethyl 2-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenoxy]acetate

https://huagongshe.com/reaction/2249637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant(2,4-Diisobutoxyphenyl)(3-hydroxy-4-isobutoxyphenyl)methanoneHCID 17816454—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenoxy]acetateHCID 17816467—

Reaction Conditions

Temperature85 °C

Reaction Steps

In 9 ml of N,N-dimethylformamide is dissolved 0.86 g of (2,4-diisobutoxyphenyl)(3-hydroxy-4-isobutoxyphenyl)methanone, to which is added 0.12 g of 60% sodium hydride. After elevating the temperature to 80° C., 0.52 ml of ethyl 2-bromoacetate is added, and the mixture thus obtained is stirred at 80-90° C. for 30 minutes. The reaction mixture is cooled to ambient temperature and added to a mixture of ethyl acetate and water, pH is adjusted to 2 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; hexane:ethyl acetate=5:1) to obtain 1.00 g of ethyl 2-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenoxy]acetate as a light yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-56bb2acbc1a2485c88f799498f1c4126
Source noteuspto-grants-2008_01