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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Bromo-1,3-diethyl-5-methylbenzene | HCID 11579491 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (2,6-diethyl-4-methylphenyl)glyoxylate | HCID 56942718 | 98.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09029295B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-3bf67bda3de445bfa502a9bf6bbafd3c |
|---|
| Source note | uspto-grants-2015_05 |
|---|