HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954473Generated: October 31, 2026
Diethyl Oxalate → ETHYL 2-METHYLBENZOYLFORMATE
https://huagongshe.com/reaction/1954473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 178424304 | HCID 178424304 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ETHYL 2-METHYLBENZOYLFORMATE | HCID 11622483 | 87% |
Reaction Steps
A solution of diethyl oxalate (30 g) in anhydrous THF (300 ml) was cooled to -30° C. A solution of o-tolyl magnesium chloride in THF (1 M, 140 ml) was added to the above solution at a temperature of the reaction solution of -20° C. After stirring at -30° C. for 30 minutes, the mixture was allowed to warm up to 0° C. and combined with an aqueous ammonium chloride solution. The mixture was concentrated under reduced pressure. The residue was treated with water and diethyl ether and phases were separated. The organic phase was washed with water, dried over anhydrous magnesium sulfate and concentrated to give a yellow oil. The oil was subjected to silica gel column chromatography (eluent: hexane/ethyl acetate=10/1) to give the desired ethyl 2-methylbenzoylformate (18 g, yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06121476 |
|---|
| Source dataset | uspto-grants-2000_09 |
|---|
| ORD ID | ord-bfbfc1da1f074ca59cd62d54dd676d1a |
|---|
| Source note | uspto-grants-2000_09 |
|---|