戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 261034作成日:2026年10月27日

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

https://huagongshe.com/reaction/261034

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl methylmalonateHCID 11857—
反応物2,4-DichloronitrobenzeneHCID 11899—
反応物Sodium hydrideHCID 24758—
溶媒WaterHCID 962—
溶媒HexamethylphosphoramideHCID 12679—
生成物Propanedioic acid, 2-(3-chloro-4-nitrophenyl)-2-methyl-, 1,3-diethyl esterHCID 12854241—

反応手順

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.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04163788
出典データセットuspto-grants-1979_08
ORD IDord-721bb9578c3e4c2f825b13a29fdb3719
出典メモuspto-grants-1979_08