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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571618Generated: October 31, 2026

Hydrochloric Acid → Ethyl (2,6-diethyl-4-methylphenyl)glyoxylate

https://huagongshe.com/reaction/571618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl OxalateHCID 7268—
Reactant1,1-DibromoethaneHCID 11201—
ReactantMagnesiumHCID 5462224—
Reactant2-Bromo-1,3-diethyl-5-methylbenzeneHCID 11579491—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (2,6-diethyl-4-methylphenyl)glyoxylateHCID 5694271898.1%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a 3 L volume four-necked flask, magnesium (turnings, 35.31 g), tetrahydrofuran (anhydrous, 600 ml) were added under nitrogen atmosphere at room temperature. After the stirring was started, the mixture was heated to about 30° C. of the internal temperature, and then dibromoethane (25.4 g) was added dropwise over 20 minutes. The resulting mixture was stirred for 30 minutes, and heated to about 50° C. of the internal temperature. To the mixture was added a solution of 2,6-diethyl-4-methylbromobenzene (300.18 g) in tetrahydrofuran (150 ml) dropwise over 2 hours. The resulting mixture was stirred at 50° C. for 1 hour, and then diethyl oxalate (192.5 g) was added dropwise at about 0° C. over 15 minutes. The resulting mixture was stirred at room temperature for 2 hours. To the mixture was added 3.5 weight % of hydrochloric acid (1000 ml) and concentrated hydrochloric acid (60 ml) with cooling. Then, the organic layer was evaporated, and the aqueous layer was extracted with tert-butyl methyl ether. The organic layer was concentrated under reduced pressure to give 320.82 g of ethyl (2,6-diethyl-4-methylphenyl)glyoxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029295B2
Source datasetuspto-grants-2015_05
ORD IDord-3bf67bda3de445bfa502a9bf6bbafd3c
Source noteuspto-grants-2015_05