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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78255생성일: 2026년 10월 23일

Benzyl Bromide → 2-Benzyl-5-[1,3]dioxolan-2-yl-pyridine

https://huagongshe.com/ko/reaction/78255

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물2-Bromo-5-(1,3-dioxolan-2-YL)pyridineHCID 18469668—
촉매ZincHCID 23994—
촉매Nickel, dichlorobis(triphenylphosphine)-HCID 498315—
용매TetrahydrofuranHCID 8028—
생성물2-Benzyl-5-[1,3]dioxolan-2-yl-pyridineHCID 5925510862%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841327B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b6bf6bbb3365446e850cc2a709bc1add
출처 메모uspto-grants-2014_09