참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Allyl iodide | HCID 11166 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone | HCID 58604073 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone | HCID 58604046 | — |
반응 단계
NaH (0.32 g of a 60% dispersion in mineral oil, 8.0 mmol) was added to an ice-cold solution of 2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone (1.55 g, 6.7 mmol) in anhydrous DMF (30 mL). The mixture was purged with N2 and stirred at 0-5° C. for 45 minutes. Allyl iodide (0.91 mL, 10.0 mmol) was added and, after a few minutes, the cooling bath was removed and the mixture was stirred overnight at room temperature. Additional NaH (0.16 g of a 61.1% dispersion in mineral oil, 4.1 mmol) was added and the mixture was stirred at room temperature for 15 minutes. Allyl iodide (0.46 mL, 5.0 mmol) was added and the mixture was stirred at room temperature for 24 hours. The mixture was partitioned between EtOAc and water, and the aqueous phase was back-extracted with several portions of EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered, and concentrated under vacuum. The residue was purified by Biotage™ (Charlottesville, Va.) flash chromatography on a 40M (4×15 cm) silica gel column, eluting with 1% to 4% EtOAc in hexane, to afford 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone as an 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-4ffa97b3f8e743c692bc0288aacb38db |
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| 출처 메모 | uspto-grants-2008_10 |
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