HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555663Generated: October 30, 2026
Dimethyl malonate → HCID 66986518, compound
https://huagongshe.com/reaction/555663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 4-fluoro-3-nitrobenzoate | HCID 21277355 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 66986518 | HCID 66986518 | — |
Reaction Steps
30 mL of anhydrous dimethyl sulfoxide was added to 0.98 g of sodium hydride defatted with hexane, and to the resulting solution, 2.98 g of dimethyl malonate was gradually added at room temperature while stirring. After completion of the dropwise addition, the resulting mixture was stirred at 100° C. for 1 hour. This mixture was cooled to room temperature, and 3 g (14 mmol) of ethyl 4-fluoro-3-nitrobenzoate was added thereto, and the resulting mixture was stirred at room temperature for 30 minutes and then further stirred at 100° C. for 1 hour. After the reaction mixture was cooled, saturated ammonium chloride was added thereto, and the resulting mixture was subjected to extraction with ethyl acetate. The obtained ethyl acetate layer was washed sequentially with saturated brine and water, dried over anhydrous sodium sulfate and then evaporated to dryness under reduced pressure, whereby ethyl 4-(di(methoxycarbonyl)methyl)-3-nitrobenzoate was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053461B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-993e6cd21ad849dfb176144efecebc89 |
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| Source note | uspto-grants-2011_11 |
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