HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930118Generated: November 1, 2026
Ethoxalyl chloride → HCID 59627701, compound
https://huagongshe.com/reaction/1930118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 1-Chloro-2-methoxy-4-methylbenzene | HCID 99352 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59627701 | HCID 59627701 | 52.1% |
Reaction Steps
Ethyl 2-chloro-2-oxoacetate (6.43 mL, 57.47 mmol) was added dropwise to a stirred suspension of aluminum trichloride (7.66 g, 57.47 mmol) in DCM (60 mL) at 0° C., over a period of 5 minutes under nitrogen. The resulting suspension was stirred at 0° C. for 15 minutes. A solution of 1-chloro-2-methoxy-4-methylbenzene (5 g, 31.93 mmol) in DCM (50 mL) was added dropwise over a period of 5 minutes and the resulting mixture was stirred at 0° C. for 90 minutes. The reaction mixture was cautiously quenched with water (300 mL) at 0° C., extracted with EtOAc (2×200 mL), the organic layers were combined, dried over MgSO4, filtered and evaporated to afford cream solid. The crude solid was triturated with DCM to give a solid which was collected by filtration and dried under vacuum to give ethyl 2-(5-chloro-4-methoxy-2-methylphenyl)-2-oxoacetate (4.27 g) as a white solid. The residue was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford ethyl 2-(5-chloro-4-methoxy-2-methylphenyl)-2-oxoacetate (1.85 g,) as a white solid. Total yield of ethyl 2-(5-chloro-4-methoxy-2-methylphenyl)-2-oxoacetate (6.12 g, 74.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188092B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-c8dc2bddd7a64d3e9dfa31b14fb4555b |
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| Source note | uspto-grants-2012_05 |
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