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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1359362생성일: 2026년 10월 27일

Ammonium Chloride → 2-Benzyl-6-(3-pyrroline-1-yl)pyridine

https://huagongshe.com/reaction/1359362

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-Bromo-6-(pyrrolidin-1-yl)pyridineHCID 15470277—
반응물2-Bromo-6-(3-pyrroline-1-yl)pyridineHCID 18182355—
반응물HCID 178418336HCID 178418336—
촉매Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
용매TetrahydrofuranHCID 8028—
생성물2-Benzyl-6-(3-pyrroline-1-yl)pyridineHCID 18182236—

반응 단계

72.3 ml of a tetrahydrofuran solution containing 1.07 mol of benzylmagnesium chloride was added dropwise into a mixture of 11.6 g of a mixture of 2-bromo-6-(3-pyrroline-1-yl)pyridine and 2-bromo-6-(pyrrolidine-1-yl)pyridine and 20 ml of tetrahydrofuran containing 1.4 g of 1,3-bis(diphenylphosphino)propanenickel(II) chloride over 10 minutes in an ice bath. After cooling at room temperature overnight, the reaction solution was poured into aqueous saturated ammonium chloride and extracted with ethyl acetate. The organic phase was washed with aqueous saturated sodium chloride and the solvent was removed. The residue was subjected to NH-silica gel (Fuji Silicia) column chromatography and eluted with hexane and then with hexane/ethyl acetate (20:1), to give 11.8 g of the title compound as a mixture with 2-benzyl-6-(pyrrolidine-1-yl)pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06599917B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-17112d273d1749f8ab8152601b38eabf
출처 메모uspto-grants-2003_07