HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442791Generated: October 25, 2026
Monoethyl malonate → Ethyl 3-methoxy-4-methoxycarbonylbenzoylacetate
https://huagongshe.com/reaction/442791
Participants
| Role | Name | HCID | Charge |
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| Reactant | Monoethyl malonate | HCID 70615 | — |
| Reactant | 3-Methoxy-4-methoxycarbonylbenzoyl chloride | HCID 15161968 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Ethyl 3-methoxy-4-methoxycarbonylbenzoylacetate | HCID 53689794 | — |
Reaction Steps
To a solution of ethyl hydrogen malonate (4.38 g, 33.2 mmol) in dry tetrahydrofuran (100 ml) cooled under an atmosphere of nitrogen to -60° C. with efficient stirring was added a solution of n-butyllithium in hexane (2.5M, 26.5 ml) rapidly dropwise, allowing the temperature to rise to -10° C. during the addition. After stirring the resulting suspension for 15 min at -10° C. it was recooled to -70° C. and a solution of 3-methoxy-4-methoxycarbonylbenzoyl chloride (4.46 g, 19.5 mmol) in dry tetrahydrofuran (30 ml) added dropwise. After addition, the reaction mixture was allowed to warm to room temperature and after 1 h diluted with cold aqueous hydrochloric acid (2M, 35 ml) and ice. The mixture was extracted with diethyl ether (200 ml) and the extract washed twice with a saturated solution of sodium bicarbonate, water and a saturated solution of sodium chloride. The organic layer was dried over magnesium sulphate, filtered and evaporated. The residue was purified on flash silica eluting with dichloromethane to give ethyl 3-methoxy-4-methoxycarbonylbenzoylacetate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891899 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-3f77f296a0f74d6180ea08ed8755bd36 |
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| Source note | uspto-grants-1999_04 |
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