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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2390121생성일: 2026년 10월 25일

Triethylamine → Tert-butyl{4-chloro-2-[(4-methylpyridin-3-yl)ethynyl]phenoxy}acetate

https://huagongshe.com/reaction/2390121

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Bromo-4-methylpyridineHCID 817630—
반응물Tert-butyl(4-chloro-2-ethynylphenoxy)acetateHCID 56594381—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl{4-chloro-2-[(4-methylpyridin-3-yl)ethynyl]phenoxy}acetateHCID 58521948—

반응 조건

온도60 °C

반응 단계

A mixture of 3-bromo-4-methylpyridine (Apollo; 355 mg; 2.06 mmol), tert-butyl(4-chloro-2-ethynylphenoxy)acetate (Intermediate 3, 500 mg; 1.87 mmol), dichlorobis(triphenylphosphine)palladium(II) (82 mg; 0.11 mmol), copper(I) iodide (21 mg; 0.11 mmol) was degassed during two minutes under nitrogen then THF (7.5 mL) and triethylamine (520 μL; 3.75 mmol) were added and reaction mixture was stirred at 60° C. for 16 hours. The solvents were removed under vacuum affording a dark brown residue, which was purified by flash column chromatography (silica), eluting with cyclohexane containing increasing amounts of EtOAc. The title compound was obtained as a dark brown sticky solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273769B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-8dfc4f7844f243e2a372e3758a0ac0ef
출처 메모uspto-grants-2012_09