참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzyl Bromide | HCID 7498 | — |
| 반응물 | 2-Bromo-5-(1,3-dioxolan-2-YL)pyridine | HCID 18469668 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 촉매 | Bis(triphenylphosphine)nickel(II)chloride | HCID 84306 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-Benzyl-5-[1,3]dioxolan-2-yl-pyridine | HCID 59255108 | 62% |
반응 단계
To a suspension of zinc (5.0 g, 77 mmol, highly reactive Rieke metal, 100 mL tetrahydrofuran suspension) and tetrahydrofuran (300 mL) was added dropwise benzyl bromide (7.9 mL, 66 mmol) at 0° C., which was stirred for 4 hours at the same temperature. To this suspension were added bis(triphenylphosphine)nickel (II) chloride (5.8 g, 8.8 mmol) and 2-bromo-5-[1,3]dioxolan-2-yl-pyridine (11 g, 49 mmol) described in Manufacturing Example 210-1-2, which was stirred for another 2 hours at room temperature. The reaction solution was partitioned into ethyl acetate and an ammonium chloride aqueous solution. The organic layer was separated and concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=2:1, 1:1) to obtain the title compound (7.3 g, 62%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07691882B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-308f12e17f5049c1a5d03c380b37e6cc |
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| 출처 메모 | uspto-grants-2010_04 |
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