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HRID 11571作成日:2026年10月23日

Acetamidomalonic acid diethyl ester → Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate

https://huagongshe.com/ja/reaction/11571

反応式

関与物質

役割名称HCID仕込み量
反応物Acetamidomalonic acid diethyl esterHCID 14041—
反応物Benzene, 2-(bromomethyl)-1-methoxy-3-nitro-HCID 186047—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物Diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonateHCID 2197461580.8%

反応手順

Sodium metal (1.15 g) was dissolved in absolute ethanol (500 mL), and to the resulting solution was added diethyl 2-acetylaminomalonate (9.1 g). After 15 min at room temperature, a solution of 2-methoxy-6-nitrobenzyl bromide (J. Med. Chem. 1977, 20, 190–196) (8.6 g) in tetrahydrofuran (25 mL) was added over 2 min. After 16 h stirring at room temperature the mixture was evaporated. The residue was dissolved in a mixture of ethyl acetate and water. The ethyl acetate layer was separated and washed sequentially with water and brine before drying over anhydrous sodium sulfate. Evaporation was followed by silica gel chromatography eluting initially with dichloromethane, followed by ethyl acetate, to obtain diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate (10.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098235B2
出典データセットuspto-grants-2006_08
ORD IDord-f049805b02c647ba9683e13a05b400db
出典メモuspto-grants-2006_08