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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857810Generated: November 3, 2026

Ethyl Bromide → Ethyl 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-oxoacetate

https://huagongshe.com/reaction/1857810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantMagnesiumHCID 5462224—
Reactant1-Bromo-2-(1-ethoxyethyl)oxymethyl-benzeneHCID 15483785—
ReactantEthanedioic acid, monoethyl esterHCID 21943339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-oxoacetateHCID 1539047068.4%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixed solution of 1-bromo-2-(1-ethoxyethyl)oxymethylbenzene (3.11 g, 0.012 mol) and dry THF (10 ml) was added dropwise at 50 to 60° C. over 25 minutes to a solution prepared by adding dry THF (2 ml) and ethyl bromide (0.2 ml) to magnesium (0.44 g, 0.018 mol) in a stream of nitrogen. After completion of the addition, the mixture was stirred at 50 to 60° C. for 1 hour and cooled to room temperature. After cooling, the mixture was added dropwise to a mixed solution of ethyl oxalate (2.63 g, 0.018 mol) and dry THF (30 ml) at below -50° C. over 15 minutes. Then, the mixture was stirred at -50 to -60° C for 1 hour. After completion of the reaction, water (200 ml) was added, and the mixture was extracted with ether (200 ml). The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to obtain ethyl 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-oxoacetate (2.30 g, Yield: 68.4%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147231
Source datasetuspto-grants-2000_11
ORD IDord-0a105e18b7134ab89133823d5fdef14e
Source noteuspto-grants-2000_11