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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379421생성일: 2026년 10월 24일

Acetic Acid → N-benzyl-6-chloro-4-o-tolyl-nicotinamide

https://huagongshe.com/ko/reaction/379421

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물N-Benzyl-6-chloro-nicotinamideHCID 857488—
반응물HCID 178424304HCID 178424304—
촉매Manganese triacetate dihydrateHCID 12416832—
용매TetrahydrofuranHCID 8028—
생성물N-benzyl-6-chloro-4-o-tolyl-nicotinamideHCID 1216731489.1%

반응 조건

온도0 °C

반응 단계

A solution of 0.5 g (2.0 mMol) N-benzyl-6-chloro-nicotinamide in 5.0 ml THF was added over 25 minutes to 10.1 ml (10.1 mMol) of o-tolylmagnesium chloride solution (1M in THF) cooled to 0° C. After 2.5 hours stirring at room temperature, the reaction mixture was cooled again to 0° C. and 4.0 ml acetic acid were added over 15 minutes followed by 1.1 g (4.1 mMol) manganese triacetate dihydrate. After stirring for 1 hour at room temperature, the reaction mixture was filtered and the filtrate was poured onto 20 ml deionized water. Sodium bicarbonate was added portionwise to bring the pH to 7 and the phases were separated. The aqueous layer was extracted with dichloromethane. The combined organic extracts were washed with water, dried (Na2SO4) and evaporated. The residue was purified by flash chromatography (eluent ethyl acetate/n-hexane 2:1) to yield 0.6 g (88%) N-benzyl-6-chloro-4-o-tolyl-nicotinamide as an orange resin.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06297375B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-9c1004844e1743f5ab97ad94b3f4675d
출처 메모uspto-grants-2001_10