Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6498생성일: 2026년 10월 24일
N-Methoxy-N-methylbenzamide → 1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-one
https://huagongshe.com/ko/reaction/6498
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Methoxy-N-methylbenzamide | HCID 569575 | — |
| 반응물 | 3-(4-(Dimethylamino)benzyloxy)phenylacetylene | HCID 19388226 | — |
| 반응물 | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Phenyl-3-[3-(4-(dimethylamino)benzyloxy)phenyl]-2-propyne-1-one | HCID 19388218 | — |
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 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. Purify by silica gel chromatography to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05248825 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-1dcbf41e8a1e4ec0990437ca83de30a4 |
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| 출처 메모 | uspto-grants-1993_09 |
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