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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858586Generated: October 30, 2026

Potassium Carbonate → 3-(4-propoxyphenyl)propanoic acid

https://huagongshe.com/reaction/858586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
ReactantMethyl 3-(2-hydroxyphenyl)propionateHCID 2794569—
SolventDimethylformamideHCID 6228—
Product3-(4-propoxyphenyl)propanoic acidHCID 225593598.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of methyl 3-(hydroxyphenyl)propionate (15 g, 83.24 mmol) and iodopropane (12.14 mL, 124.5 mmol) in DMF (80 mL) was added K2CO3 (34 g, 249.7 mmol). The resultant slurry was stirred vigorously and heated to 60° C. under argon for 12 h. DMF was evaporated and residue partitioned between EtOAC and 1N HCl. The organic layer was washed with H2O, and brine then dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (10% EtOAc in hexanes) to provide the desired product (17 g, 98%) as a clear oil. The resultat oil was dissolved in THF (150 mL), and 2M NaOH (68 mL) was added. The reaction was stirred overnight at room temperature. THF was evaporated and residue acidified with concentrated HCl and extracted 3 times with EtOAC, (100 mL). The organic layer was washed with H2O, dried over Na2SO4 and concentrated to a white solid which was recrystalized from hexanes to provide the desired product (14.06 g 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-f570dba210964d789c8431bb48670f5d
Source noteuspto-grants-2006_12