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HRID 261034Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/261034

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl methylmalonateHCID 11857—
Edukt2,4-DichloronitrobenzeneHCID 11899—
EduktSodium hydrideHCID 24758—
LösungsmittelWaterHCID 962—
LösungsmittelHexamethylphosphoramideHCID 12679—
ProduktPropanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl esterHCID 12854241—

Reaktionsschritte

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.)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04163788
Quelldatensatzuspto-grants-1979_08
ORD IDord-721bb9578c3e4c2f825b13a29fdb3719
Quellennotizuspto-grants-1979_08