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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171617Generated: November 1, 2026

Hydrochloric Acid → 2-(3-(Hydroxymethyl)phenyl)acetic acid

https://huagongshe.com/reaction/2171617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCalcium CarbonateHCID 10112—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(3-(bromomethyl)phenyl)acetateHCID 10563066—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2-(3-(Hydroxymethyl)phenyl)acetic acidHCID 1498095264.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Calcium carbonate (11 g) was added to a mixture of ethyl[3-(bromomethyl)phenyl]acetate (4.56 g), dioxane (70 ml) and water (70 ml), followed by stirring at 80° C. for 6 hours. EtOAc and water were added to the reaction mixture, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc). The purified product thus obtained was mixed with EtOH (50 ml), and a 1M aqueous NaOH solution (35 ml) was added thereto, followed by stirring at room temperature for 1 hour. 1M hydrochloric acid (35 ml) was added to the reaction mixture, followed by concentration under reduced pressure. MeOH and Na2SO4 were added to the obtained residue, and the insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure to obtain [3-(hydroxymethyl)phenyl]acetic acid (1.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051283B2
Source datasetuspto-grants-2015_06
ORD IDord-24ec1bcbfa544c9ea678cc4aac849791
Source noteuspto-grants-2015_06