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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295921Generated: October 29, 2026

Dimethylformamide → Ethyl 5-bromo-2-ethoxy-4-methylbenzoate

https://huagongshe.com/reaction/1295921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant5-bromo-2-hydroxy-4-methylbenzoic acidHCID 243934—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-bromo-2-ethoxy-4-methylbenzoateHCID 22929763—

Reaction Conditions

Temperature50 °C

Reaction Steps

After dissolving 5-bromo-2-hydroxy-4-methylbenzoic acid (9.35 g) in dimethylformamide, potassium carbonate (14 g) and ethyl iodide (8 ml) were added in that order and the mixture was stirred at 50° C. for 3 hours. It was then diluted with ethyl acetate, washed with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated to yield ethyl 5-bromo-2-ethoxy-4-methylbenzoate. The product was dissolved in ethanol (100 ml), 5 N sodium hydroxide (20 ml) was added and the mixture was heated to reflux for 30 minutes. After adding 5 N hydrochloric acid (25 ml) for neutralization, extraction was performed with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, filtered and concentrated to yield the title compound (10.4 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-a77b0601025942b6bf398b731656b7d4
Source noteuspto-grants-2007_07