Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602272Generated: October 30, 2026

Cesium carbonate → 2-Iodo-5-(4-methoxybenzyloxy)benzoic acid 4-methoxybenzyl ester

https://huagongshe.com/reaction/602272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Hydroxy-2-iodobenzoic acidHCID 1238003—
SolventAcetonitrileHCID 6342—
Product2-Iodo-5-(4-methoxybenzyloxy)benzoic acid 4-methoxybenzyl esterHCID 5968425330%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 2-iodo-5-hydroxybenzoic acid (prepared according to the method described in J. Am. Chem. Soc., 1984, 106, 2651) (27.15 g, 103 mmol) in anhydrous acetonitrile (400 mL) was added cesium carbonate (73.80 g, 227 mmol) and 4-methoxybenzyl chloride (33.5 mL, 247 mmol). The resulting solid mass was broken up and the mixture heated at 65° C. for 15 h. The reaction mixture was poured into sat. NaHCO3 (aq.) (400 mL) and the resultant mixture extracted with ethyl acetate (3×300 mL). The combined organic extracts were washed with brine (300 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by chromatography on silica gel with a gradient of ethyl acetate:hexanes (1:9, v/v) to ethyl acetate:hexanes (1:3, v/v) as eluent to afford 2-iodo-5-(4-methoxybenzyloxy)benzoic acid 4-methoxybenzyl ester (15.39 g, 30.52 mmol, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906504B2
Source datasetuspto-grants-2011_03
ORD IDord-57b23c6daf574c829662b2069cd348f0
Source noteuspto-grants-2011_03