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HRID 217909作成日:2026年10月26日

Ammonia → 4-(4-Methoxyphenyl)butanamide

https://huagongshe.com/reaction/217909

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Carbon DioxideHCID 280—
反応物MethanolHCID 887—
反応物Sodium ChlorideHCID 5234—
反応物4-MethylmorpholineHCID 7972—
反応物Isobutyl chloroformateHCID 62365—
反応物4-(4-Methoxyphenyl)butyric acidHCID 78280—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-Methoxyphenyl)butanamideHCID 22566175—

反応条件

温度-15 °C

反応手順

4-(4-Methoxyphenyl) butyric acid (1) (450 g, 2.32 mole) was combined with dry THF (4 L) and 4-methylmorpholine (268 mL, 2.43 mole) in a 12 L three neck flask with mechanical stirring, an ice-methanol cooling bath and nitrogen atmosphere. Small pieces of dry ice were used to bring the bath temperature below −20° C. Isobutyl chloroformate was added at a rate so as not to exceed an internal temperature of −10° C. After stirring for 30 min. at −10 to −20° C., a 4.7 M solution of ammonia in methanol (990 mL, 4.64 mole) was added in one portion. During the addition, the reaction temperature rose to 0° C. The reaction was allowed to stir for 30 min. and then allowed to stand overnight. The product mixture was transferred to a 22 L separatory funnel with ethyl acetate (6 L), and 10% sodium chloride solution (1.5 L). The layers were separated and the organic solution was washed with 10% sodium chloride solution (4×1 L) and then brine (3×500 mL). The organic layer was dried over sodium sulfate, filtered, evaporated and placed under high vacuum overnight. This afforded 432 g (97%) of the pure amide (117) as an off white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198286B2
出典データセットuspto-grants-2012_06
ORD IDord-d785aa70ceed406db48bb0a054bfb2c2
出典メモuspto-grants-2012_06