참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Methoxy-N-methylbenzamide | HCID 569575 | — |
| 반응물 | 1-Ethynyl-3-((4-methoxybenzyl)oxy)benzene | HCID 15281122 | — |
| 반응물 | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Phenyl-3-[3-(4-methoxybenzyloxy)phenyl]-2-propyne-1-one | HCID 9840975 | — |
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
| 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-d099e8b2015d49a88b10fcd0cbfb9273 |
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| 출처 메모 | uspto-grants-1993_09 |
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