Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Phenylacetylene → 1-(3,4,5-Trimethoxyphenyl)-3-phenyl-2-propyne-1-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Phenylacetylene | HCID 10821 | — |
| 반응물 | N,3,4,5-tetramethoxy-N-methyl-Benzamide | HCID 267535 | — |
| 반응물 | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(3,4,5-Trimethoxyphenyl)-3-phenyl-2-propyne-1-one | HCID 14763389 | 34.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05248825 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-49f779f24ab24cde9206b27accb4fa10 |
| 출처 메모 | uspto-grants-1993_09 |