HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261034Generated: October 25, 2026
Diethyl methylmalonate → Propanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl ester
https://huagongshe.com/reaction/261034
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | 2,4-Dichloronitrobenzene | HCID 11899 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | Propanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl ester | HCID 12854241 | — |
Reaction Steps
The starting material can also be prepared as follows: 4.8 g 50% sodium hydride in mineral oil are added to 100 ml hexamethylphosphoramide while stirring under nitrogen. Hereupon 17.1 g diethyl α-methylmalonate are added and the mixture slowly heated to 100°. The solution of 19.2 g 2,4-dichloro-nitrobenzene in 20 ml hexamethylphosphoramide is added dropwise during 1/2 hour and the temperature kept at 100° for seven hours. After cooling, the mixture is diluted with water, concentrated in vacuo, the residue taken up in water and extracted with benzene. The extract is washed with water, dried, filtered, evaporated, the residue distilled and the fraction boiling at 147°-148°/0.25 mm Hg collected, to yield the diethyl α-methyl-α-(3-chloro-4-nitrophenyl)-malonate. (The analogously prepared diethyl α-ethyl-α-(3-chloro-4-nitrophenyl)-malonate boils at 170°-174°/1 mm Hg.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04163788 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-721bb9578c3e4c2f825b13a29fdb3719 |
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| Source note | uspto-grants-1979_08 |
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