돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8225생성일: 2026년 10월 23일

4-Methylbenzyl chloride → 1-(6-Methylpyridin-2-yl)-2-p-tolyl-ethanone

https://huagongshe.com/ko/reaction/8225

반응식

참여 물질

역할이름HCID투입량
반응물4-Methylbenzyl chlorideHCID 7722—
반응물MagnesiumHCID 5462224—
반응물N-methoxy-N,6-dimethylpyridine-2-carboxamideHCID 45869585—
촉매1,2-DibromoethaneHCID 7839—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물1-(6-Methylpyridin-2-yl)-2-p-tolyl-ethanoneHCID 21992900—

반응 조건

온도50 °C

반응 단계

To a slurry of magnesium turnings (406 mg, 16.7 mmol) in toluene (10 mL) is added 4-methylbenzylchloride (10 mg, 0.06 mmol) dropwise in tetrahydrofuran (0.2 mL). Two drops of 1,2-dibromoethane are added, the mixture heated to 50° C., and allowed to cool to room temperature. This process is repeated until reaction initiates. 4-Methylbenzylchloride (1.5 g, 10 mmol) in tetrahydrofuran (7 mL) is added slowly while keeping the internal temperature below 32° C. After the addition is complete the reaction is stirred at room temperature for 1 h. The reaction mixture is added dropwise over 5 minutes to a solution of 6-methyl-pyridine-2-carboxylic acid methoxy-methyl-amide (Prep 250, 1 g, 5.6 mmol) in toluene (5 mL). The reaction is stirred for an additional 45 minutes. The reaction is quenched with 1 N hydrochloric acid and stirred for 30 minutes. The aqueous layer is neutralized with saturated sodium bicarbonate and extracted twice with ethyl acetate. The combined organic extracts are washed with brine, dried (sodium sulfate), filtered and concentrated in vacuo. The crude residue is chromatographed on SiO2 (50% ethyl acetate/hexane to 75% ethyl acetate/hexane) to yield the title compound, 633 mg (25%), as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087626B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-4bc2f7f0f41d432a9827529aae96896e
출처 메모uspto-grants-2006_08