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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61926Generated: October 25, 2026

Iodoethane → 2-(2-Bromo-5-methoxy-phenyl)-2-ethyl-butyric acid

https://huagongshe.com/reaction/61926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
Reactant15-Crown-5HCID 36336—
ReactantMethyl (2-bromo-5-methoxyphenyl)acetateHCID 10658910—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(2-Bromo-5-methoxy-phenyl)-2-ethyl-butyric acidHCID 66835356—

Reaction Conditions

Temperature140 °C

Reaction Steps

(2-Bromo-5-methoxy-phenyl)-acetic acid methyl ester (3.51 g, 13.5 mmol) was dissolved in DMF (4.5 ml), and added with NaH (2.1 g, 67.7 mmol). Subsequently, 15-crown-5 (1.38 ml, 6.8 mmol) and EtI (5.5 ml, 67.7 mmol) cooled to 0° C. were added to the mixture. The mixture was diluted with ethyl acetate and washed with water and saturated brine. The residues obtained after concentration under reduced pressure were purified by silica gel column (hexane-ethyl acetate). Then, the resultant was dissolved in ethanol (80 ml) and water (80 ml), added with KOH (91 g), and stirred at 140° C. The reaction solution was extracted with ethyl acetate, and washed with water and saturated brine. After concentration under reduced pressure, the target compound was obtained (10.62 g, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440922B2
Source datasetuspto-grants-2016_09
ORD IDord-d12d0702602249d3b4e6de3021d0b768
Source noteuspto-grants-2016_09