Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358187Generated: October 30, 2026

Ethyl 2-bromopropionate → HCID 14721691, compound

https://huagongshe.com/reaction/358187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-bromopropionateHCID 79040—
ReactantHCID 23693411HCID 23693411—
SolventEthanolHCID 702—
ProductHCID 14721691HCID 1472169185.2%

Reaction Steps

In 100 ml of ethanol was dissolved 10.0 g. (0.05 mole) of sodium 2,4-dichloro-3-methylphenolate. With stirring at room temperature, 9.1 g (0.05 mole) of ethyl 2-bromopropionate was added. The mixture was heated under relfux for 4 hours. The ethanol was distilled off under reduced pressure, and the residue was extracted with 50 ml of diethyl ether. The ethereal layer was washed with 25 ml of a 5% aqueous solution of sodium hydroxide and 25 ml of water, and dried over anyhdrous magnesium sulfate. The dessicant was removed by filtration, and the diethyl ether was distilled off to give 11.8 g of crude ethyl 2-(2,4-dichloro-3-methylphenoxy)propionate. The crude ester (11.8 g) was dissolved in 100 ml of glacial acetic acid. Concentrated hydrochloric acid (25 ml) was added, and the mixture was stirred at 100° C. for 40 minutes. The reaction mixture was cooled, and poured onto 300 ml of ice water. The precipitated crystals were filtered, washed with water, and dried to give 9.2 g of 2-(2,4-dichloro-3-methylphenoxy)-propionic acid. The yield was 73.9% based on the sodium 2,4-dichloro-3-methylphenolate, and the final product had a melting point of 149.5 to 150.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465507
Source datasetuspto-grants-1984_08
ORD IDord-668e2eed2cfd444984985459dbb4ebed
Source noteuspto-grants-1984_08