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HRID 1757510생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1757510

반응식

참여 물질

역할이름HCID투입량
반응물N-Methoxy-N-methylbenzamideHCID 569575—
반응물3-(4-(Dimethylamino)benzyloxy)phenylacetyleneHCID 19388226—
반응물Lithium bis(trimethylsilyl)amideHCID 57426343—
용매TetrahydrofuranHCID 8028—
생성물1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-oneHCID 19388218—

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-(dimethylamino)benzyloxy)phenylacetylene (0.51 g, 2 mmol) in tetrahydrofuran and stir the solution for 45 minutes at 0° C. Add N-methoxy-N-methylbenzamide (0.4 g, 2.4 mmol), remove the cooling bath andstir 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. Purifyby silica gel chromatography to give the title compound. Alternatively, compounds of formula (1) can be prepared according to the procedure set forth in Scheme B, wherein all substituents, unless otherwise indicated, are previously described. ##STR3##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05446068
출처 데이터셋uspto-grants-1995_08
ORD IDord-811a5c27251840fcad575856719bd0b2
출처 메모uspto-grants-1995_08