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HRID 4779作成日:2026年10月24日

Salicylamide → 2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamide

https://huagongshe.com/ja/reaction/4779

反応式

関与物質

役割名称HCID仕込み量
反応物SalicylamideHCID 5147—
反応物o-Toluenesulfonyl chlorideHCID 8623—
反応物Sodium amideHCID 24533—
反応物1-Methyl-3-pyrrolidinolHCID 93074—
反応物Sodium MethoxideHCID 10942334—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物2-[(1-Methyl-3-pyrrolidinyl)oxy]benzamideHCID 13726283—

反応条件

温度70 °C

反応手順

To 85.6 g (2.2 moles) of sodium amide in 1.5 liter of dry toluene was added 202 g (2 moles) of 1-methyl-3-pyrrolidinol so as not to exceed a temperature of 50° C. The mixture was then heated to 70° C. for 4.5 hours. The mixture was cooled and 381 g (2 moles) of o-toluenesulfonylchloride was added at a rapid drop while maintaining a temperature of 20°-30° C. with an ice bath. The mixture was stirred at room temperature for 2.5 hours and washed with water. The toluene solution was dried with sodium sulfate and concentrated. The residue, dissolved in 500 ml of dimethylformamide, was added to a reaction mixture prepared by adding 119 g (2.2 moles) of sodium methoxide and 274 g (2.0 moles) of salicylamide to one liter of dimethylformamide and the mixture was worked up as in preparation 1. Yield of product was 170 g (38%), m.p. 116°-118° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727152
出典データセットuspto-grants-1988_02
ORD IDord-b0c0fc9ef6e847a68cadcb68fa16fa36
出典メモuspto-grants-1988_02