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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6488생성일: 2026년 10월 24일

N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one

https://huagongshe.com/ko/reaction/6488

반응식

참여 물질

역할이름HCID투입량
반응물N-Methoxy-N-methylbenzamideHCID 569575—
반응물1-Ethynyl-3-((4-methoxybenzyl)oxy)benzeneHCID 15281122—
반응물Lithium bis(trimethylsilyl)amideHCID 57426343—
용매TetrahydrofuranHCID 8028—
생성물1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-oneHCID 9840975—

반응 조건

온도0 °C

반응 단계

Place lithium hexamethyldisilazane (2 mL of a 1M solution in tetrahydrofuran, 2 mmol) and tetrahydrofuran (8 mL) under an argon atmosphere and cool to 0° C. Add a solution of 3-(4-methoxybenzyloxy)phenylacetylene (0.48 g, 2 mmol) in tetrahydrofuran and stir the brown solution for 45 minutes at 0° C. Add N-methoxy-N-methylbenzamide (0.4 g, 2.4 mmol), remove the cooling bath and stir at room temperature for 1 hour. Partition the mixture between ethyl ether and water, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo to yield an oil. Filter through silica gel and elute with 10% ethyl acetate/hexane to yield a crude solid. Recrystallize (hexane, ethyl ether) to yield 0.26 g (1st crop) and 0.15 g (2nd crop) of the title compound; mp 79°-80° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248825
출처 데이터셋uspto-grants-1993_09
ORD IDord-d099e8b2015d49a88b10fcd0cbfb9273
출처 메모uspto-grants-1993_09