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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 422275생성일: 2026년 10월 26일

Triphenylphosphine → 2-(4-(5-phenyl-2H-tetrazol-2-yl)but-1-ynyl)pyridine

https://huagongshe.com/reaction/422275

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물5-Phenyl-1H-tetrazoleHCID 87425—
반응물4-(Pyridin-2-yl)but-3-yn-1-olHCID 11008063—
용매DichloromethaneHCID 6344—
생성물2-(4-(5-phenyl-2H-tetrazol-2-yl)but-1-ynyl)pyridineHCID 1164478051%

반응 조건

온도0 °C

반응 단계

A mixture of 5-phenyl-2H-tetrazole (330 mg, 2.2 mmol), 4-(pyridin-2-yl)but-3-yn-1-ol (220 mg, 1.49 mmol) and triphenylphosphine polymer supported (750 mg, 2.2 mmol, loading 3 mmol/g) were dissolved DCM (3 mL) and stirred at 0° C. Diisoprpylazodicarboxylate (452 mg, 2.2 mmol) was added dropwise, at 0° C. over a period of 30 min The reaction mixture was then warmed to room temperature and stirred over night. The reaction mixture was filtered through celite and the cake was washed with DCM. The combined organic layers were washed with aqueous ammoniac, brine, dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (prepacked 25 g silicagel column, DCM 100% as eluent) to afford 209 mg of 2-(4-(5-phenyl-2H-tetrazol-2-yl)but-1-ynyl)pyridine (Yield: 51%) as a pink powder (M.P.=71-73° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101637B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-771725ecc09441d494661c29d66887de
출처 메모uspto-grants-2012_01