돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542759생성일: 2026년 10월 27일

m,alpha-Dichlorotoluene → 3-(2-(3-Chlorophenyl)ethyl)-N-(1,1-dimethylethyl)-2-pyridinecarboxamide

https://huagongshe.com/reaction/542759

반응식

참여 물질

역할이름HCID투입량
반응물m,alpha-DichlorotolueneHCID 12103—
반응물Sodium BromideHCID 253881—
반응물N-tert-Butyl-3-methylpyridine-2-carboxamideHCID 5463796—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물3-(2-(3-Chlorophenyl)ethyl)-N-(1,1-dimethylethyl)-2-pyridinecarboxamideHCID 1412869592%

반응 조건

온도-40 °C

반응 단계

31.5 g of N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide (e.g., as prepared in step A of Example I above) is dissolved in 600 mL of dry tetrahydrofuran and the resulting solution is cooled to -40° C. Two equivalents of n-butyllithium in hexane are added while the temperature is maintained at -40° C. The solution turned deep purple-red. 1.6 g of sodium bromide is added and the mixture is stirred. A solution of 26.5 g (0.174 mole) m-chlorobenzylchloride in 125 mL of tetrahydrofuran is added while the temperature is maintained at -40° C. The reaction mixture is stirred until the reaction is complete as determined by thin layer chromatography. Water is added to the reaction until the color is dissipated. The reaction mixture is extracted with ethyl acetate, washed with water, and concentrated to a residue. A yield of 92% for the product is shown by chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04659716
출처 데이터셋uspto-grants-1987_04
ORD IDord-87fac8ba9bb44990afdb80cc3b5fb68c
출처 메모uspto-grants-1987_04