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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249627Generated: October 26, 2026

Hydrochloric Acid → 2-[5-(4-Isobutoxy-2-isopentyloxybenzoyl)-2-isobutoxyphenyl]acetic acid

https://huagongshe.com/reaction/2249627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-[5-(4-isobutoxy-2-isopentyloxybenzoyl)-2-isobutoxyphenyl]acetateHCID 17816460—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[5-(4-Isobutoxy-2-isopentyloxybenzoyl)-2-isobutoxyphenyl]acetic acidHCID 1781653255.5%

Reaction Steps

In 2 ml of methanol is dissolved 0.13 g of methyl 2-[5-(4-isobutoxy-2-isopentyloxybenzoyl)-2-isobutoxyphenyl]acetate, to which is added 0.2 ml of 5 mol/L solution of sodium hydroxide. The mixture thus obtained is stirred at ambient temperature for one hour and then at 50-60° C. for one hour. Chloroform and water are added to the reaction mixture, pH is adjusted to 2 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer 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=2:1) to obtain 0.07 g of 2-[5-(4-isobutoxy-2-isopentyloxybenzoyl)-2-isobutoxyphenyl]acetic acid as a white-colored solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-79dcd215ec464b2d928b85f2e81bcbd7
Source noteuspto-grants-2008_01