참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| 반응물 | 4-(4-Bromophenyl)-3-(4-methoxyphenyl)butan-2-one | HCID 66923703 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-Bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one | HCID 86650847 | 82.8% |
반응 단계
Diisopropylamine (0.084 g, 0.83 mmol) was dissolved in anhydrous diethyl ether (7.5 mL) under argon atmosphere and cooled to −78° C. BuLi (0.52 mL, 0.83 mmol) was added dropwise to the solution and the resulting solution was allowed to warm to 0° C. for 10 min, then recooled to −78° C. TMS-Cl (freshly distilled over calcium hydride, 0.11 mL, 0.83 mmol) was added dropwise to the solution at −78° C., after addition, the reaction was allowed to stir for an additional 10 min. The solution was then cooled to −90° C., and 4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one (0.25 g, 0.75 mmol) was added dropwise as a solution in anhydrous diethyl ether. After addition was complete, the solution was allowed to stir for an additional 40 min. The reaction was then warmed to 0° C. and phenyltrimethylammonium tribromide (0.31 mg, 0.83 mmol) was slowly added dropwise as a solution in anhydrous THF (4 mL). The resulting solution was allowed to stir at 25° C. for 1 hour. The mixture was diluted with EtOAc and water, washed with NaCl (×3), dried over sodium sulfate and concentrated in vacuo. The crude product was purified using silica gel chromatography (0-30% EtOAc in hexanes gradient) to afford 256 mg of 1-bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one as a viscous oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08492387B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-e34228de24764d1881609c1a56dad532 |
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| 출처 메모 | uspto-grants-2013_07 |
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