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HRID 379421作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物N-Benzyl-6-chloro-nicotinamideHCID 857488—
反応物HCID 178424304HCID 178424304—
触媒Manganese triacetate dihydrateHCID 12416832—
溶媒TetrahydrofuranHCID 8028—
生成物N-benzyl-6-chloro-4-o-tolyl-nicotinamideHCID 1216731489.1%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297375B1
出典データセットuspto-grants-2001_10
ORD IDord-9c1004844e1743f5ab97ad94b3f4675d
出典メモuspto-grants-2001_10