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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447327Generated: October 26, 2026

Diethyl methylmalonate → Propanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl ester

https://huagongshe.com/reaction/1447327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl methylmalonateHCID 11857—
Reactant2,4-DichloronitrobenzeneHCID 11899—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventHexamethylphosphoramideHCID 12679—
ProductPropanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316850
Source datasetuspto-grants-1982_02
ORD IDord-3a8f5a9632cf41078ea36258e93765c9
Source noteuspto-grants-1982_02