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HRID 640539作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/640539

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物2-Bromo-5-(1,3-dioxolan-2-YL)pyridineHCID 18469668—
触媒ZincHCID 23994—
触媒Bis(triphenylphosphine)nickel(II)chlorideHCID 84306—
溶媒TetrahydrofuranHCID 8028—
生成物2-Benzyl-5-[1,3]dioxolan-2-yl-pyridineHCID 5925510862%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691882B2
出典データセットuspto-grants-2010_04
ORD IDord-308f12e17f5049c1a5d03c380b37e6cc
出典メモuspto-grants-2010_04