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HRID 257100作成日:2026年10月27日

2,2,2'-Trimethylpropionanilide → 2,2-Dimethyl-N-[2-[2-methylamino-2-(2-methylphenyl)ethyl]phenyl]propanamide

https://huagongshe.com/reaction/257100

反応式

関与物質

役割名称HCID仕込み量
反応物2,2,2'-TrimethylpropionanilideHCID 2734005—
反応物(E)-N-Methyl-1-(2-methylphenyl)methanimineHCID 12451890—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2,2-Dimethyl-N-[2-[2-methylamino-2-(2-methylphenyl)ethyl]phenyl]propanamideHCID 15085941—

反応手順

A chilled solution (-4° C.) of 126 g of 2,2-dimethyl-N-[(2-methyl)phenyl]propanamide in 900 ml of tetrahydrofuran was treated dropwise over 1.5 hr with n-butyl lithium (500 ml of a 2.5M solution in hexanes). After the addition was complete, the resulting solution was stirred for 1 hr, with cooling, and was then treated over 0.5 hr with a solution of 91.77 g of 2-methylbenzaldehyde methyl imine. The reaction mixture was quenched by rapid addition of water. After concentration the residue was extracted with dichloromethane. The combined organic extract was dried over anhydrous sodium sulfate, filtered and concentrated. A 50 g portion of the residue (213 g) was acidified with 10% hydrochloric acid and partitioned with toluene. The aqueous layer was basified with a 50% sodium hydroxide solution and extracted with dichloromethane. The organic layer was dried over anhydrous sodium sulfate and concentrated. Upon standing under nitrogen overnight in a refrigerator a solid formed, which was triturated with hexane to give 2,2-dimethyl-N-[2 -[2-methylamino-2-(2-methylphenyl)ethyl]phenyl]propanamide, mp 77°-79° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260339
出典データセットuspto-grants-1993_11
ORD IDord-6aac3a45d85e478593865e2ab42e6ed3
出典メモuspto-grants-1993_11