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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2216370생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2216370

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물MagnesiumHCID 5462224—
반응물2-Bromo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridineHCID 21942269—
반응물HCID 178419663HCID 178419663—
촉매Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-Benzyl-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridineHCID 21942262—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07112593B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-7efc740474614fa8bb53d2db1bac1da8
출처 메모uspto-grants-2006_09