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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249616Generated: November 2, 2026

Hydrochloric Acid → 2-{5-[(2,4-Diisobutoxyphenyl)(hydroxy)methyl]-2-isobutoxyphenyl}-acetic acid

https://huagongshe.com/reaction/2249616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium ChlorideHCID 433294—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[5-(2,4-Diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acidHCID 17816564—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product2-{5-[(2,4-Diisobutoxyphenyl)(hydroxy)methyl]-2-isobutoxyphenyl}-acetic acidHCID 5768438049.8%

Reaction Conditions

Temperature55 °C

Reaction Steps

In 2 ml of methanol is dissolved 100 mg of 2-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl]acetic acid. After adding 18 mg of sodium borohydride at 5-10° C., the mixture thus obtained is stirred at 50-60° C. for one hour. Then, 40 mg of sodium borohydride and 40 mg of lithium chloride are further added at ambient temperature, and the mixture thus obtained is stirred at 50-60° C. for two hours. Chloroform and water are added to the reaction mixture, pH is adjusted to 2.0 with 2 mol/L hydrochloric acid, and the organic layer is separated. The organic layer is successively washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. Thus, 50 mg of 2-{5-[(2,4-diisobutoxyphenyl)(hydroxy)methyl]-2-isobutoxyphenyl}-acetic acid is obtained as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-4925ea3363ae4cd391512edc94ca8433
Source noteuspto-grants-2008_01