참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl iodide | HCID 10962 | — |
| 반응물 | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone | HCID 58604073 | — |
반응 단계
A mixture of 6-methoxy-3,4-dihydro-1(2H)-naphthalenone (400 mg, 2.27 mmol), iodobutane (0.284 mL, 2.5 mmol), NaH (98 mg of a 61.1% dispersion in mineral oil, 2.5 mmol), and anhydrous tetrahydrofuran (THF, 1 mL) was placed under a N2 atmosphere and stirred at room temperature for 15.5 hours. The mixture was partitioned between EtOAc (20 mL) and water (30 mL) containing 2N HCl (3 mL). The organic phase was washed with brine (20 mL), dried over MgSO4, filtered, and evaporated under vacuum to afford an oil. The crude product was purified by preparative layer chromatography on five 0.1×20×20 cm silica gel GF plates (Analtech, Newark, Del.), developing with CH2Cl2. The UV visible product band was eluted with EtOAc and the eluant evaporated under vacuum to provide 2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone as a clear oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07432284B2 |
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| 출처 데이터셋 | uspto-grants-2008_10 |
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| ORD ID | ord-7d06554a428c4e888c8f720f297954f1 |
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| 출처 메모 | uspto-grants-2008_10 |
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