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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257100생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/257100

반응식

참여 물질

역할이름HCID투입량
반응물2,2,2'-TrimethylpropionanilideHCID 2734005—
반응물(E)-N-Methyl-1-(2-methylphenyl)methanimineHCID 12451890—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2,2-Dimethyl-N-[2-[2-methylamino-2-(2-methylphenyl)ethyl]phenyl]propanamideHCID 15085941—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260339
출처 데이터셋uspto-grants-1993_11
ORD IDord-6aac3a45d85e478593865e2ab42e6ed3
출처 메모uspto-grants-1993_11