참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| 반응물 | 2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromide | HCID 2724168 | — |
| 반응물 | 3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propene | HCID 53923275 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene | HCID 19694130 | — |
| 생성물 | Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene | HCID 70113689 | — |
반응 단계
(E and Z)-3-(1,3-Dioxan-2-yl)-1-(2-pyridyl)-1-propene (148 and 149). To a suspension of 4.6 g (10.2 mmol) of [2-(1,3-dioxan-2-yl)ethyl]triphenylphosphonium bromide (Aldrich Chemical Co.) in 50 mL of THF at 0° C. was added 6.4 mL (10.2 mmol) of n-butyl lithium (1.6M in hexanes) and the resulting red solution was allowed to stir at 0° C. for 0.5 h. To this solution was added 880 μL (9.3 mmol) of 2-pyridinecarboxaldehyde (Aldrich Chemical Co.). The reaction mixture was allowed to stir at room temperature for 1 h and was then poured into water and partitioned with ether. The combined either extracts were dried over MgSO4 and concentrated. Flash chromatography (elution with 3:1 hexane:ethyl acetate) gave 0.43 g of E-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1 -propene (148) and 1.12 g of Z-3-(1,3-dioxan-2-yl)-1-(2-pyridyl)-1-propene (149). 1H NMRs consistent with structures.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05620971 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-321cdd4893b44debad54cad867cbe1e8 |
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| 출처 메모 | uspto-grants-1997_04 |
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