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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1359358생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1359358

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-ethylenedioxypyrrolidine-1-yl)pyridine, 240 mg of 1,3-bis (diphenylphosphino)propanenickel (II) chloride and 20 ml of tetrahydrofuran was stirred in an ice bath in a nitrogen atmosphere. Into the mixture were 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 at room temperature overnight as it was. The reaction solution was partitioned between an aqueous saturated ammonium chloride solution and ethyl acetate. The organic phase was washed with brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography using 5-10% ethyl acetate/hexane, to give 6.6 g of the target compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06599917B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-79150b776aed4c589b81009d95e16a17
출처 메모uspto-grants-2003_07