HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375409Generated: October 25, 2026
Diethyl Oxalate → Ethyl (3,5-dimethoxyphenyl)(oxo)acetate
https://huagongshe.com/reaction/1375409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1-Iodo-3,5-dimethoxybenzene | HCID 640179 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (3,5-dimethoxyphenyl)(oxo)acetate | HCID 24722256 | 71% |
Reaction Steps
To a solution of 5.28 g (20 mmol) of 1-iodo-3,5-dimethoxybenzene (W. Riedhl, F. Imhof, Justus Liebigs Ann. Chem., 1955;597:153–157) in 100 mL of THF at −78° C. is added 12.3 mL (21 mmol) of 1.7 M tert-BuLi in pentane, and after a further 5 minutes 4.4 g (30 mmol) of diethyl oxalate is added. After being allowed to warm to −20° C., the mixture is quenched with aqueous NH4Cl, and the THF is removed under vacuum. Work-up in EtOAc, followed by chromatography on silica, eluting with hexane/EtOAc (9:1) gives 3.38 g (71%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169778B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-48ca9cf45c6341f980a2dca74a1702f5 |
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| Source note | uspto-grants-2007_01 |
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