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HRID 2216370作成日:2026年10月27日

Benzyl Bromide → 2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine

https://huagongshe.com/reaction/2216370

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MagnesiumHCID 5462224—
反応物2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridineHCID 21942269—
反応物HCID 178419663HCID 178419663—
触媒Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridineHCID 21942262—

反応手順

A mixture of 6.3 g of 2-bromo-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridine, 240 mg of 1,3-bis(diphenylphosphino)propanenickel (II) chloride and 20 ml of tetrahydrofuran was stirred in advance under nitrogen atmosphere in an ice bath. To this was added dropwise a diethyl ether solution of benzyl magnesium bromide prepared from 3.4 ml of benzyl bromide, 0.8 g of magnesium and 15 ml of diethyl ether, followed by stirring as it was at room temperature for overnight. The reaction mixture was partitioned between a saturated aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography with 5–10% ethyl acetate/hexane, to give 6.6 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07112593B2
出典データセットuspto-grants-2006_09
ORD IDord-7efc740474614fa8bb53d2db1bac1da8
出典メモuspto-grants-2006_09