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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6490생성일: 2026년 10월 23일

Phenylacetylene → 1-(3,4,5-Trimethoxyphenyl)-3-phenyl-2-propyne-1-one

https://huagongshe.com/ko/reaction/6490

반응식

참여 물질

역할이름HCID투입량
반응물PhenylacetyleneHCID 10821—
반응물N,3,4,5-tetramethoxy-N-methyl-BenzamideHCID 267535—
반응물Lithium bis(trimethylsilyl)amideHCID 57426343—
용매TetrahydrofuranHCID 8028—
생성물1-(3,4,5-Trimethoxyphenyl)-3-phenyl-2-propyne-1-oneHCID 1476338934.9%

반응 단계

Place lithium hexamethyldisilazane (3 mL of a 1M solution in tetrahydrofuran, 3 mmol) and tetrahydrofuran (10 mL) under an argon atmosphere and cool to 0° C. Add phenylacetylene (0.33 mL, 3 mmol) and stir at 0° C. for 30 minutes. Add N-methoxy-N-methyl-(3,4,5-trimethoxy)benzamide (0.76 g, 3 mmol), remove the cooling bath and stir at room temperature for 1 hour. Partition between ethyl ether and saturated aqueous sodium chloride, separate the organic phase and dry (MgSO4). Filter and evaporate the solvent in vacuo. Pour onto silica gel and elute with 20% ethyl acetate/hexane to yield a crude solid. Recrystallize (hexane/ethyl acetate) to yield 0.31 g of the title compound; mp 94°-96° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248825
출처 데이터셋uspto-grants-1993_09
ORD IDord-49f779f24ab24cde9206b27accb4fa10
출처 메모uspto-grants-1993_09