참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| 반응물 | 1-(2,5-Difluoro-4-methoxyphenyl)piperidin-4-one | HCID 23111466 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-(2,5-Difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidine | HCID 23111400 | 34.1% |
반응 단계
A reaction vessel was charged with methoxymethyltriphenyl-phosphonium chloride (1.114 g), the atomosphere indide the vessel was substituted with nitrogen, and anhydrous tetrahydrofuran (2 mL) was added, followed by further dropwise addition of 1.57 M n-butyl lithium-in-hexane solution (2 mL) at room temperature and thereafter 10 minutes' stirring at room temperature. To the reaction mixture a mixture of 1-(2,5-difluoro-4-methoxyphenyl)piperidin-4-one (676 mg) and anhydrous tetrahydrofuran (0.5 mL) was added dropwise, followed by 30 minutes' stirring at room temperature. To the reaction mixture water was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline solution and dried over anhydrous sodium sulfate. Distilling the solvent off, the crude product as obtained was purified on silica gel column chromatography (eluent, hexane: ethyl acetate=10:1) to provide 1-(2,5-difluoro-4-methoxyphenyl)-4-methoxymethylenepiperidine (257 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07449466B2 |
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| 출처 데이터셋 | uspto-grants-2008_11 |
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| ORD ID | ord-0354f4e12ffe4f7cad2355f89c6f816a |
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| 출처 메모 | uspto-grants-2008_11 |
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